Reference Source

E A Currim Pvt Ltd · 99-39 · INDIA

For E A Currim 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 Umber SF Supplement; product code is 54 A - - 99 Vitamin, N.E.C; date published is 10/02/2015; address is Ground Floor , 19 Kazi Sayed St , Mumbai, Maharashtra INDIA, verified against its source on 2026-09-16.

Firm
E A Currim Pvt Ltd verified
Import alert
99-39
Import alert name
Detention Without Physical Examination of Imported Food Products That Appear to Be Misbranded
Country
INDIA verified
Address
Ground Floor , 19 Kazi Sayed St , Mumbai, Maharashtra INDIA verified
Date published
10/02/2015 verified
Product code
54 A - - 99 Vitamin, N.E.C. verified
Product
Umber SF Supplement verified
FDA notes
Product is labeled as a dietary supplement but fails to bear nutrition labeling ("Supplement Facts" panel) as required by Section 403(q)(5)(F) and 21 CFR 101.36. Product is misbranded within the meaning of Section 403(i)(2) of the Act because the label fails to list each ingredient, specifically, the capsule ingredients, in the ingredient statement (21 CFR 101.4(a)(1)). The label fails to identify the product using the term "dietary supplement" as part of the statement of identity on the principal display panel (21 CFR 101.3(a) and (g)). The product fails to provide the appropriate "Disclaimer" in accordance with 21 CFR 101.93(a-e). verified
Sourceaccessdata.fda.gov
Verified
Review by
DatasetFDA import alert red lists: firms subject to detention without physical examination

What the source says

E A Currim Pvt Ltd Date Published : 10/02/2015 Ground Floor , 19 Kazi Sayed St , Mumbai, Maharashtra INDIA 54 A - - 99 Vitamin, N.E.C. Date Published: 10/02/2015 Desc: Umber SF Supplement Notes: Product is labeled as a dietary supplement but fails to bear nutrition labeling ("Supplement Facts" panel) as required by Section 403(q)(5)(F) and 21 CFR 101.36. Product is misbranded within the meaning of Section 403(i)(2) of the Act because the label fails to list each ingredient, specifically, the capsule ingredients, in the ingredient statement (21 CFR 101.4(a)(1)). The label fails to identify the product using the term "dietary supplement" as part of the statement of identity on the principal display panel (21 CFR 101.3(a) and (g)). The product fails to provide the appropriate "Disclaimer" in accordance with 21 CFR 101.93(a-e).

accessdata.fda.gov, retrieved 2026-09-15

Source

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