# M/S Svatv Herbs India Pvt. Ltd. · 99-39 · INDIA — FDA import alert red lists: firms subject to detention without physical examination

For M/S Svatv Herbs India Pvt. Ltd. · 99-39 · INDIA, import alert is 99-39; import alert name is Detention Without Physical Examination of Imported Food Products That Appear to Be Misbranded; country is INDIA; product is Svatv Bhumi Amla Powder | Giloy Powder | Shatavari Powder | Beet Root Powder; product code is 54 - - - -- Vitamins/Minerals (Human/Animal); Proteins/Unconv Dietary Supp (Human) | 54 - - - -- Vitamins/Minerals (Human/Animal); Proteins/Unconv Dietary Supp (Human) | 54 - - - -- Vitamins/Minerals (Human/Animal); Proteins/Unconv Dietary Supp (Human) | 54 - - - -- Vitamins/Minerals (Human/Animal); Proteins/Unconv Dietary Supp (Human); date published is 08/26/2025; address is 1st Floor , B - 25 , New Delhi, Delhi INDIA, verified against its source on 2026-09-16.

- **Firm:** M/S Svatv Herbs India Pvt. Ltd. _(verified: appears in the quote below)_
- **Import alert:** 99-39
- **Import alert name:** Detention Without Physical Examination of Imported Food Products That Appear to Be Misbranded
- **Country:** INDIA _(verified: appears in the quote below)_
- **Address:** 1st Floor , B - 25 , New Delhi, Delhi INDIA _(verified: appears in the quote below)_
- **Date published:** 08/26/2025 _(verified: appears in the quote below)_
- **Product code:** 54 - - - -- Vitamins/Minerals (Human/Animal); Proteins/Unconv Dietary Supp (Human) | 54 - - - -- Vitamins/Minerals (Human/Animal); Proteins/Unconv Dietary Supp (Human) | 54 - - - -- Vitamins/Minerals (Human/Animal); Proteins/Unconv Dietary Supp (Human) | 54 - - - -- Vitamins/Minerals (Human/Animal); Proteins/Unconv Dietary Supp (Human) _(verified: each item appears in the quote below)_
- **Product:** Svatv Bhumi Amla Powder | Giloy Powder | Shatavari Powder | Beet Root Powder _(verified: each item appears in the quote below)_
- **FDA notes:** The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the product appears to be misbranded within the meaning of: Section 403(q)(5)(f). The products do not present nutrition information on the labeling (21 CFR 101.36). Section 403(y). Labels fail to bear a domestic address or domestic phone number (complete street address or phone number) through which the responsible person may receive a report of a serious adverse event with such dietary supplements (section 761 of the Act [21 U.S.C. 379aa-1]). Section 403(s)(2)(B). Labels fail to include the statement of identity as a “dietary supplement” on the principal display panel, except that the word “dietary” may be deleted and replaced by the name of the dietary ingredients in the product or an appropriately descriptive term indicating the type of dietary ingredients that are in the product [21 CFR 101.3(a), (b), and (g)]. “Food Supplement” is not appropriate because it does not identify or describe the dietary ingredients or combination of ingredients that the dietary supplement product supplies (62 FR 49826, 49827). | The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the product appears to be misbranded within the meaning of: Section 403(q)(5)(f). The products do not present nutrition information on the labeling as required by 21 CFR 101.36. Product fails to express the quantitative amounts of (b)(3)-dietary ingredients in metric measures using appropriate units (21 CFR 101.36(b)(3)(ii)(A)). Missing heading of “% Daily Value,” (21 CFR 101.36(b)(3)(iv)). Section 403(y). Labels fail to bear a domestic address or domestic phone number (complete street address or phone number) through which the responsible person may receive a report of a serious adverse event with such dietary supplements (section 761 of the Act [21 U.S.C. 379aa-1]). Section 403(s)(2)(B). Missing statement of identity as a “dietary supplement” on the principal display panel (21 CFR 101.3(a), (b), and (g)). “Food Supplement” is not appropriate because it does not identify or describe the dietary ingredients or combination of ingredients that the dietary supplement product supplies (62 FR 49826, 49827). Section 403(i)(2). Label fails to declare the common or usual names of each ingredient used as required by 21 CFR 101.36 and 21 CFR 101.4. “Giloy Stem Powder…(Tinospora Cordifolia)” whereas the standardized common name (SCN) is “Indian tinospora” for Tinospora cordifolia according to the reference Herbs of Commerce. Section 403(q)(1)(A). Label fails to include an accurate serving size in accordance with 21 CFR 101.36(b). Should be maximum amount consumed per eating occasion as recommended in 21 CFR 101.9(b) and 21 CFR 101.12(b) Table 2. Directions of use is to take 1g-5g per day, but serving size is 1tsp (1.8g). Section 403(q)(1)(B). Incorrect number of servings per container (21 CFR 101.36(b)(1)(ii)). Label states net quantity of 227 grams (g) but declares “126126” servings per container with a serving size of 1tsp (1.8 g). | The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the product appears to be misbranded within the meaning of: Section 403(q)(5)(f). The products do not present nutrition information on the labeling as required by 21 CFR 101.36. Product fails to place the subheading “Servings Per Container” under the subheading “Serving Size,” (21 CFR 101.36(b)(1)) Section 403(y). Labels fail to bear a domestic address or domestic phone number (complete street address or phone number) through which the responsible person may receive a report of a serious adverse event with dietary supplements (section 761 of the Act [21 U.S.C. 379aa-1]). Section 403(s)(2)(B). Labels fail to include the statement of identity as a “dietary supplement” on the principal display panel, except that the word “dietary” may be deleted and replaced by the name of the dietary ingredients in the product or an appropriately descriptive term indicating the type of dietary ingredients that are in the product [21 CFR 101.3(a), (b), and (g)]. “Food Supplement” is not appropriate because it does not identify or describe the dietary ingredients or combination of ingredients that the dietary supplement product supplies (62 FR 49826, 49827). Section 403(s)(2)(C). Label fails to identify the part of the plant (e.g., root, leaves) from which each botanical dietary ingredient in the product is derived, as required by 21 CFR 101.4(h)(1). If the entire or whole plant is used, then that information must be declared. Section 403(q)(1)(B). Label states a net quantity of contents of 227 g, but declares 227 servings per container with a serving size of “1/2 tsp [teaspoon] (2 g).” | The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the product appears to be misbranded within the meaning of: Section 403(q)(5)(f). The products do not present nutrition information on the labeling (21 CFR 101.36). Section 403(y). Labels fail to bear a domestic address or domestic phone number through which the responsible person may receive a report of a serious adverse event with such dietary supplements. “Domestic address or domestic phone number,” means a complete street address or phone number (section 761 of the Act [21 U.S.C. 379aa-1]). Section 403(s)(2)(B). Labels fail to include the statement of identity as a “dietary supplement” on the principal display panel, except that the word “dietary” may be deleted and replaced by the name of the dietary ingredients in the product or an appropriately descriptive term indicating the type of dietary ingredients that are in the product [21 CFR 101.3(a), (b), and (g)]. This statement of identity shall be placed on the products labels’ principal display panel (PDP), as required by 21 CFR 101.3(a). Please note that the term “Food Supplement” is not appropriate because it does not identify or describe the dietary ingredients or combination of ingredients that the dietary supplement product supplies (see 62 FR 49826, 49827). _(verified: each item appears in the quote below)_

## What the source says

> M/S Svatv Herbs India Pvt. Ltd. Date Published : 08/26/2025 1st Floor , B - 25 , New Delhi, Delhi INDIA 54 - - - -- Vitamins/Minerals (Human/Animal); Proteins/Unconv Dietary Supp (Human) Date Published: 08/26/2025 Desc: Svatv Bhumi Amla Powder Notes: The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the product appears to be misbranded within the meaning of: Section 403(q)(5)(f). The products do not present nutrition information on the labeling (21 CFR 101.36). Section 403(y). Labels fail to bear a domestic address or domestic phone number (complete street address or phone number) through which the responsible person may receive a report of a serious adverse event with such dietary supplements (section 761 of the Act [21 U.S.C. 379aa-1]). Section 403(s)(2)(B). Labels fail to include the statement of identity as a “dietary supplement” on the principal display panel, except that the word “dietary” may be deleted and replaced by the name of the dietary ingredients in the product or an appropriately descriptive term indicating the type of dietary ingredients that are in the product [21 CFR 101.3(a), (b), and (g)]. “Food Supplement” is not appropriate because it does not identify or describe the dietary ingredients or combination of ingredients that the dietary supplement product supplies (62 FR 49826, 49827). 54 - - - -- Vitamins/Minerals (Human/Animal); Proteins/Unconv Dietary Supp (Human) Date Published: 08/26/2025 Desc: Giloy Powder Notes: The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the product appears to be misbranded within the meaning of: Section 403(q)(5)(f). The products do not present nutrition information on the labeling as required by 21 CFR 101.36. Product fails to express the quantitative amounts of (b)(3)-dietary ingredients in metric measures using appropriate units (21 CFR 101.36(b)(3)(ii)(A)). Missing heading of “% Daily Value,” (21 CFR 101.36(b)(3)(iv)). Section 403(y). Labels fail to bear a domestic address or domestic phone number (complete street address or phone number) through which the responsible person may receive a report of a serious adverse event with such dietary supplements (section 761 of the Act [21 U.S.C. 379aa-1]). Section 403(s)(2)(B). Missing statement of identity as a “dietary supplement” on the principal display panel (21 CFR 101.3(a), (b), and (g)). “Food Supplement” is not appropriate because it does not identify or describe the dietary ingredients or combination of ingredients that the dietary supplement product supplies (62 FR 49826, 49827). Section 403(i)(2). Label fails to declare the common or usual names of each ingredient used as required by 21 CFR 101.36 and 21 CFR 101.4. “Giloy Stem Powder…(Tinospora Cordifolia)” whereas the standardized common name (SCN) is “Indian tinospora” for Tinospora cordifolia according to the reference Herbs of Commerce. Section 403(q)(1)(A). Label fails to include an accurate serving size in accordance with 21 CFR 101.36(b). Should be maximum amount consumed per eating occasion as recommended in 21 CFR 101.9(b) and 21 CFR 101.12(b) Table 2. Directions of use is to take 1g-5g per day, but serving size is 1tsp (1.8g). Section 403(q)(1)(B). Incorrect number of servings per container (21 CFR 101.36(b)(1)(ii)). Label states net quantity of 227 grams (g) but declares “126126” servings per container with a serving size of 1tsp (1.8 g). 54 - - - -- Vitamins/Minerals (Human/Animal); Proteins/Unconv Dietary Supp (Human) Date Published: 08/26/2025 Desc: Shatavari Powder Notes: The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the product appears to be misbranded within the meaning of: Section 403(q)(5)(f). The products do not present nutrition information on the labeling as required by 21 CFR 101.36. Product fails to place the subheading “Servings Per Container” under the subheading “Serving Size,” (21 CFR 101.36(b)(1)) Section 403(y). Labels fail to bear a domestic address or domestic phone number (complete street address or phone number) through which the responsible person may receive a report of a serious adverse event with dietary supplements (section 761 of the Act [21 U.S.C. 379aa-1]). Section 403(s)(2)(B). Labels fail to include the statement of identity as a “dietary supplement” on the principal display panel, except that the word “dietary” may be deleted and replaced by the name of the dietary ingredients in the product or an appropriately descriptive term indicating the type of dietary ingredients that are in the product [21 CFR 101.3(a), (b), and (g)]. “Food Supplement” is not appropriate because it does not identify or describe the dietary ingredients or combination of ingredients that the dietary supplement product supplies (62 FR 49826, 49827). Section 403(s)(2)(C). Label fails to identify the part of the plant (e.g., root, leaves) from which each botanical dietary ingredient in the product is derived, as required by 21 CFR 101.4(h)(1). If the entire or whole plant is used, then that information must be declared. Section 403(q)(1)(B). Label states a net quantity of contents of 227 g, but declares 227 servings per container with a serving size of “1/2 tsp [teaspoon] (2 g).” 54 - - - -- Vitamins/Minerals (Human/Animal); Proteins/Unconv Dietary Supp (Human) Date Published: 08/26/2025 Desc: Beet Root Powder Notes: The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the product appears to be misbranded within the meaning of: Section 403(q)(5)(f). The products do not present nutrition information on the labeling (21 CFR 101.36). Section 403(y). Labels fail to bear a domestic address or domestic phone number through which the responsible person may receive a report of a serious adverse event with such dietary supplements. “Domestic address or domestic phone number,” means a complete street address or phone number (section 761 of the Act [21 U.S.C. 379aa-1]). Section 403(s)(2)(B). Labels fail to include the statement of identity as a “dietary supplement” on the principal display panel, except that the word “dietary” may be deleted and replaced by the name of the dietary ingredients in the product or an appropriately descriptive term indicating the type of dietary ingredients that are in the product [21 CFR 101.3(a), (b), and (g)]. This statement of identity shall be placed on the products labels’ principal display panel (PDP), as required by 21 CFR 101.3(a). Please note that the term “Food Supplement” is not appropriate because it does not identify or describe the dietary ingredients or combination of ingredients that the dietary supplement product supplies (see 62 FR 49826, 49827).

## Source

- https://www.accessdata.fda.gov/cms_ia/importalert_1144.html

Last verified: 2026-09-16. Review by: 2026-11-15.
Part of [FDA import alert red lists: firms subject to detention without physical examination](https://referencesource.org/fda-import-alert-red-list/).