NDC 73002-321 Pain Relief Caffeine And Hemp
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 73002-321?
What are the uses for Pain Relief Caffeine And Hemp?
Which are Pain Relief Caffeine And Hemp UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAFFEINE CITRATE (UNII: U26EO4675Q)
- CAFFEINE (UNII: 3G6A5W338E) (Active Moiety)
- CANNABIS SATIVA SUBSP. SATIVA FLOWERING TOP (UNII: 8X454SZ22D)
- CANNABIS SATIVA SUBSP. SATIVA FLOWERING TOP (UNII: 8X454SZ22D) (Active Moiety)
Which are Pain Relief Caffeine And Hemp 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- GLYCERIN (UNII: PDC6A3C0OX)
- SIRAITIA GROSVENORII FRUIT (UNII: NOU2FB51TW)
- TEA LEAF (UNII: GH42T47V24)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
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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".