NDC 69711-687 Dermamed Nutrition For Troubled Skin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69711 - Dermamed
- 69711-687 - Dermamed Nutrition For Troubled Skin
Product Characteristics
Product Packages
NDC Code 69711-687-01
Package Description: 90 g in 1 BOTTLE
Product Details
What is NDC 69711-687?
What are the uses for Dermamed Nutrition For Troubled Skin?
Which are Dermamed Nutrition For Troubled Skin UNII Codes?
The UNII codes for the active ingredients in this product are:
- VITAMIN D (UNII: 9VU1KI44GP)
- VITAMIN D (UNII: 9VU1KI44GP) (Active Moiety)
- MAGNESIUM ASPARTATE (UNII: R17X820ROL)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- THIAMINE (UNII: X66NSO3N35)
- THIAMINE ION (UNII: 4ABT0J945J) (Active Moiety)
- COPPER CU-64 (UNII: 2MK2L64N0S)
- COPPER CU-64 (UNII: 2MK2L64N0S) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- VITAMIN A (UNII: 81G40H8B0T)
- VITAMIN A (UNII: 81G40H8B0T) (Active Moiety)
Which are Dermamed Nutrition For Troubled Skin 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:
- NIACIN (UNII: 2679MF687A)
- PYRIDOXAL (UNII: 3THM379K8A)
- FOLIC ACID (UNII: 935E97BOY8)
- CITRUS BIOFLAVONOIDS (UNII: BD70459I50)
- LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
- EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
- WHEAT GERM OIL (UNII: 14C97E680P)
- FLAX SEED (UNII: 4110YT348C)
- SOYBEAN OIL (UNII: 241ATL177A)
- BORAGE OIL (UNII: F8XAG1755S)
- SELENIUM CHLORIDE (UNII: PDE7WQS0XY)
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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".