NDC 57520-0576 Dr L Advanced Hcg Formula
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What is NDC 57520-0576?
What are the uses for Dr L Advanced Hcg Formula?
Which are Dr L Advanced Hcg Formula UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHROMIUM PICOLINATE (UNII: S71T8B8Z6P)
- CHROMIUM PICOLINATE (UNII: S71T8B8Z6P) (Active Moiety)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79) (Active Moiety)
- HUMAN CHORIONIC GONADOTROPIN (UNII: 20ED16GHEB)
- HUMAN CHORIONIC GONADOTROPIN (UNII: 20ED16GHEB) (Active Moiety)
- GARCINIA CAMBOGIA FRUIT (UNII: D0QJI8UQVR)
- GARCINIA CAMBOGIA FRUIT (UNII: D0QJI8UQVR) (Active Moiety)
Which are Dr L Advanced Hcg Formula Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".