NalLife Co., Ltd. · 99-39 · THAILAND
For NalLife Co., Ltd. · 99-39 · THAILAND, import alert is 99-39; import alert name is Detention Without Physical Examination of Imported Food Products That Appear to Be Misbranded; country is THAILAND; product is Organic Soursop Graviola Leaves Capsules; product code is 54 Y - - 99 Vitamin, Mineral, Proteins and Unconventional Dietary Specialities For Humans and Animals, N.E.C; date published is 11/05/2024; address is 17/1 Moo 2 T. Ban Khao , Ranot, SONGKHLA TH-90 THAILAND, verified against its source on 2026-09-16.
- Firm
- NalLife Co., Ltd. verified
- Import alert
- 99-39
- Import alert name
- Detention Without Physical Examination of Imported Food Products That Appear to Be Misbranded
- Country
- THAILAND verified
- Address
- 17/1 Moo 2 T. Ban Khao , Ranot, SONGKHLA TH-90 THAILAND verified
- Date published
- 11/05/2024 verified
- Product code
- 54 Y - - 99 Vitamin, Mineral, Proteins and Unconventional Dietary Specialities For Humans and Animals, N.E.C. verified
- Product
- Organic Soursop Graviola Leaves Capsules verified
- 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(y) of the Act. Label fails to bear a domestic address or domestic phone number through which the responsible person, as described in section 761 of the Act, may receive a report of a serious adverse event with such dietary supplements. Section 403(s)(2)(B) of the Act. Label fails to include a 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)). Section 403(q) of the Act. Nutrition information on the label does not comply with 21 CFR 101.36 and 101.9. The title, “Supplement Facts”, is not set to full width of the nutrition label (21 CFR 101.36(e)(1)). No heavy bar separating beneath the subheading “Servings Per container” and no heavy bar beneath the last dietary ingredient (21 CFR 101.36(e)(6)(i) and (ii)). No light bar under the heading “Amount Per Serving” and “% Daily Value” (21 CFR101.36(e)(7)). % Daily Value is not under the heading “% Daily Value”, (21 CFR 101.36(b)(2)(iii)(A)). verified
What the source says
NalLife Co., Ltd. Date Published : 11/05/2024 17/1 Moo 2 T. Ban Khao , Ranot, SONGKHLA TH-90 THAILAND 54 Y - - 99 Vitamin, Mineral, Proteins and Unconventional Dietary Specialities For Humans and Animals, N.E.C. Date Published: 11/05/2024 Desc: Organic Soursop Graviola Leaves Capsules 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(y) of the Act. Label fails to bear a domestic address or domestic phone number through which the responsible person, as described in section 761 of the Act, may receive a report of a serious adverse event with such dietary supplements. Section 403(s)(2)(B) of the Act. Label fails to include a 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)). Section 403(q) of the Act. Nutrition information on the label does not comply with 21 CFR 101.36 and 101.9. The title, “Supplement Facts”, is not set to full width of the nutrition label (21 CFR 101.36(e)(1)). No heavy bar separating beneath the subheading “Servings Per container” and no heavy bar beneath the last dietary ingredient (21 CFR 101.36(e)(6)(i) and (ii)). No light bar under the heading “Amount Per Serving” and “% Daily Value” (21 CFR101.36(e)(7)). % Daily Value is not under the heading “% Daily Value”, (21 CFR 101.36(b)(2)(iii)(A)).
— accessdata.fda.gov, retrieved 2026-09-15
Source
- accessdata.fda.govhttps://www.accessdata.fda.gov/cms_ia/importalert_1144.html
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