# Eu Yan Sang (Hong Kong) Ltd. · 99-39 · HONG KONG SAR — FDA import alert red lists: firms subject to detention without physical examination

For Eu Yan Sang (Hong Kong) Ltd. · 99-39 · HONG KONG SAR, import alert is 99-39; import alert name is Detention Without Physical Examination of Imported Food Products That Appear to Be Misbranded; country is HONG KONG SAR; product is Bak Foong Pills | Bak Foong Pills | Bak Foong Pills | Bak Foong Pills; product code is 54 A - - 99 Vitamin, N.E.C. | 54 E - - 99 Herbals & Botanical Teas, N.E.C. | 54 F - - 99 Herbals & Botanicals (not Teas), N.E.C. | 66 Y - - 99 Exhibits - Other Drug Related Items N.E.C; date published is 09/27/2024; address is Yuen Long Industrial Estate Yuen Long , 10-12 Wang Lee Street , Yuen Long, New Territories HONG KONG SAR, verified against its source on 2026-09-16.

- **Firm:** Eu Yan Sang (Hong Kong) 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:** HONG KONG SAR _(verified: appears in the quote below)_
- **Address:** Yuen Long Industrial Estate Yuen Long , 10-12 Wang Lee Street , Yuen Long, New Territories HONG KONG SAR _(verified: appears in the quote below)_
- **Date published:** 09/27/2024 _(verified: appears in the quote below)_
- **Product code:** 54 A - - 99 Vitamin, N.E.C. | 54 E - - 99 Herbals & Botanical Teas, N.E.C. | 54 F - - 99 Herbals & Botanicals (not Teas), N.E.C. | 66 Y - - 99 Exhibits - Other Drug Related Items N.E.C. _(verified: each item appears in the quote below)_
- **Product:** Bak Foong Pills | Bak Foong Pills | Bak Foong Pills | Bak Foong Pills _(verified: each item appears in the quote below)_
- **FDA notes:** The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of: Sections 403(e)(1), 403(i)(2), 403(q)(5)(F), 403(s)(2)(B), and 403(y) of the Act [21 U.S.C 343(e)(1), 343(i)(2), 343(q)(5)(F), 343(s)(2)(B), and 343(y)] because the inner product label does not bear: (1) the name and place of business of the manufacturer, packer, or distributor, (2) the common or usual name of each ingredient, (3) nutrition information, (4) the statement of identity of the product, (5) a domestic address or phone number through which the responsible person (as described in section 761 of the Dietary Supplement and Nonprescription Drug Consumer Protection Act) may receive a report of a serious adverse event with such dietary supplement, and (6) any required warning statement. Section 403(f) of the Act [21 U.S.C. 343(f)] because the product label contains information in two languages, but does not repeat all the required information in both languages. Section 403(q)(1)(A) of the Act [21 U.S.C. 343(q)(1)(A)] because the Supplement Facts label (SFL) does not include all intended groups as noted in the label directions. Sections 403(q)(5)(F) of the Act [21 U.S.C. 343(q)(5)(F)] because the presentation of nutrition information on the labeling does not comply with 21 CFR 101.36, 101.9, and 101.2. | The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of: Sections 403(e)(1), 403(i)(2), 403(q)(5)(F), 403(s)(2)(B), and 403(y) of the Act [21 U.S.C 343(e)(1), 343(i)(2), 343(q)(5)(F), 343(s)(2)(B), and 343(y)] because the inner product label does not bear: (1) the name and place of business of the manufacturer, packer, or distributor, (2) the common or usual name of each ingredient, (3) nutrition information, (4) the statement of identity of the product, (5) a domestic address or phone number through which the responsible person (as described in section 761 of the Dietary Supplement and Nonprescription Drug Consumer Protection Act) may receive a report of a serious adverse event with such dietary supplement, and (6) any required warning statement. Section 403(f) of the Act [21 U.S.C. 343(f)] because the product label contains information in two languages, but does not repeat all the required information in both languages. Section 403(q)(1)(A) of the Act [21 U.S.C. 343(q)(1)(A)] because the Supplement Facts label (SFL) does not include all intended groups as noted in the label directions. Sections 403(q)(5)(F) of the Act [21 U.S.C. 343(q)(5)(F)] because the presentation of nutrition information on the labeling does not comply with 21 CFR 101.36, 101.9, and 101.2. | The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of: Sections 403(e)(1), 403(i)(2), 403(q)(5)(F), 403(s)(2)(B), and 403(y) of the Act [21 U.S.C 343(e)(1), 343(i)(2), 343(q)(5)(F), 343(s)(2)(B), and 343(y)] because the inner product label does not bear: (1) the name and place of business of the manufacturer, packer, or distributor, (2) the common or usual name of each ingredient, (3) nutrition information, (4) the statement of identity of the product, (5) a domestic address or phone number through which the responsible person (as described in section 761 of the Dietary Supplement and Nonprescription Drug Consumer Protection Act) may receive a report of a serious adverse event with such dietary supplement, and (6) any required warning statement. Section 403(f) of the Act [21 U.S.C. 343(f)] because the product label contains information in two languages, but does not repeat all the required information in both languages. Section 403(q)(1)(A) of the Act [21 U.S.C. 343(q)(1)(A)] because the Supplement Facts label (SFL) does not include all intended groups as noted in the label directions. Sections 403(q)(5)(F) of the Act [21 U.S.C. 343(q)(5)(F)] because the presentation of nutrition information on the labeling does not comply with 21 CFR 101.36, 101.9, and 101.2. | The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of: Sections 403(e)(1), 403(i)(2), 403(q)(5)(F), 403(s)(2)(B), and 403(y) of the Act [21 U.S.C 343(e)(1), 343(i)(2), 343(q)(5)(F), 343(s)(2)(B), and 343(y)] because the inner product label does not bear: (1) the name and place of business of the manufacturer, packer, or distributor, (2) the common or usual name of each ingredient, (3) nutrition information, (4) the statement of identity of the product, (5) a domestic address or phone number through which the responsible person (as described in section 761 of the Dietary Supplement and Nonprescription Drug Consumer Protection Act) may receive a report of a serious adverse event with such dietary supplement, and (6) any required warning statement. Section 403(f) of the Act [21 U.S.C. 343(f)] because the product label contains information in two languages, but does not repeat all the required information in both languages. Section 403(q)(1)(A) of the Act [21 U.S.C. 343(q)(1)(A)] because the Supplement Facts label (SFL) does not include all intended groups as noted in the label directions. Sections 403(q)(5)(F) of the Act [21 U.S.C. 343(q)(5)(F)] because the presentation of nutrition information on the labeling does not comply with 21 CFR 101.36, 101.9, and 101.2. _(verified: each item appears in the quote below)_

## What the source says

> Eu Yan Sang (Hong Kong) Ltd. Date Published : 09/27/2024 Yuen Long Industrial Estate Yuen Long , 10-12 Wang Lee Street , Yuen Long, New Territories HONG KONG SAR 54 A - - 99 Vitamin, N.E.C. Date Published: 09/27/2024 Desc: Bak Foong Pills Notes: The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of: Sections 403(e)(1), 403(i)(2), 403(q)(5)(F), 403(s)(2)(B), and 403(y) of the Act [21 U.S.C 343(e)(1), 343(i)(2), 343(q)(5)(F), 343(s)(2)(B), and 343(y)] because the inner product label does not bear: (1) the name and place of business of the manufacturer, packer, or distributor, (2) the common or usual name of each ingredient, (3) nutrition information, (4) the statement of identity of the product, (5) a domestic address or phone number through which the responsible person (as described in section 761 of the Dietary Supplement and Nonprescription Drug Consumer Protection Act) may receive a report of a serious adverse event with such dietary supplement, and (6) any required warning statement. Section 403(f) of the Act [21 U.S.C. 343(f)] because the product label contains information in two languages, but does not repeat all the required information in both languages. Section 403(q)(1)(A) of the Act [21 U.S.C. 343(q)(1)(A)] because the Supplement Facts label (SFL) does not include all intended groups as noted in the label directions. Sections 403(q)(5)(F) of the Act [21 U.S.C. 343(q)(5)(F)] because the presentation of nutrition information on the labeling does not comply with 21 CFR 101.36, 101.9, and 101.2. 54 E - - 99 Herbals & Botanical Teas, N.E.C. Date Published: 09/27/2024 Desc: Bak Foong Pills Notes: The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of: Sections 403(e)(1), 403(i)(2), 403(q)(5)(F), 403(s)(2)(B), and 403(y) of the Act [21 U.S.C 343(e)(1), 343(i)(2), 343(q)(5)(F), 343(s)(2)(B), and 343(y)] because the inner product label does not bear: (1) the name and place of business of the manufacturer, packer, or distributor, (2) the common or usual name of each ingredient, (3) nutrition information, (4) the statement of identity of the product, (5) a domestic address or phone number through which the responsible person (as described in section 761 of the Dietary Supplement and Nonprescription Drug Consumer Protection Act) may receive a report of a serious adverse event with such dietary supplement, and (6) any required warning statement. Section 403(f) of the Act [21 U.S.C. 343(f)] because the product label contains information in two languages, but does not repeat all the required information in both languages. Section 403(q)(1)(A) of the Act [21 U.S.C. 343(q)(1)(A)] because the Supplement Facts label (SFL) does not include all intended groups as noted in the label directions. Sections 403(q)(5)(F) of the Act [21 U.S.C. 343(q)(5)(F)] because the presentation of nutrition information on the labeling does not comply with 21 CFR 101.36, 101.9, and 101.2. 54 F - - 99 Herbals & Botanicals (not Teas), N.E.C. Date Published: 09/27/2024 Desc: Bak Foong Pills Notes: The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of: Sections 403(e)(1), 403(i)(2), 403(q)(5)(F), 403(s)(2)(B), and 403(y) of the Act [21 U.S.C 343(e)(1), 343(i)(2), 343(q)(5)(F), 343(s)(2)(B), and 343(y)] because the inner product label does not bear: (1) the name and place of business of the manufacturer, packer, or distributor, (2) the common or usual name of each ingredient, (3) nutrition information, (4) the statement of identity of the product, (5) a domestic address or phone number through which the responsible person (as described in section 761 of the Dietary Supplement and Nonprescription Drug Consumer Protection Act) may receive a report of a serious adverse event with such dietary supplement, and (6) any required warning statement. Section 403(f) of the Act [21 U.S.C. 343(f)] because the product label contains information in two languages, but does not repeat all the required information in both languages. Section 403(q)(1)(A) of the Act [21 U.S.C. 343(q)(1)(A)] because the Supplement Facts label (SFL) does not include all intended groups as noted in the label directions. Sections 403(q)(5)(F) of the Act [21 U.S.C. 343(q)(5)(F)] because the presentation of nutrition information on the labeling does not comply with 21 CFR 101.36, 101.9, and 101.2. 66 Y - - 99 Exhibits - Other Drug Related Items N.E.C. Date Published: 09/27/2024 Desc: Bak Foong Pills Notes: The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of: Sections 403(e)(1), 403(i)(2), 403(q)(5)(F), 403(s)(2)(B), and 403(y) of the Act [21 U.S.C 343(e)(1), 343(i)(2), 343(q)(5)(F), 343(s)(2)(B), and 343(y)] because the inner product label does not bear: (1) the name and place of business of the manufacturer, packer, or distributor, (2) the common or usual name of each ingredient, (3) nutrition information, (4) the statement of identity of the product, (5) a domestic address or phone number through which the responsible person (as described in section 761 of the Dietary Supplement and Nonprescription Drug Consumer Protection Act) may receive a report of a serious adverse event with such dietary supplement, and (6) any required warning statement. Section 403(f) of the Act [21 U.S.C. 343(f)] because the product label contains information in two languages, but does not repeat all the required information in both languages. Section 403(q)(1)(A) of the Act [21 U.S.C. 343(q)(1)(A)] because the Supplement Facts label (SFL) does not include all intended groups as noted in the label directions. Sections 403(q)(5)(F) of the Act [21 U.S.C. 343(q)(5)(F)] because the presentation of nutrition information on the labeling does not comply with 21 CFR 101.36, 101.9, and 101.2.

## 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/).