NDC 45156-5616 Inflammation Otc Radiation Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 45156 - Skin Deep
- 45156-5616 - Inflammation Otc
Product Packages
NDC Code 45156-5616-2
Package Description: 1 TUBE in 1 BOX / 29 g in 1 TUBE (45156-5616-1)
Product Details
What is NDC 45156-5616?
What are the uses for Inflammation Otc Radiation Relief?
Which are Inflammation Otc Radiation Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Inflammation Otc Radiation Relief 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- HELIANTHUS ANNUUS (UNII: BKJ0J3D1BP)
- GLYCERYL LAURATE (UNII: Y98611C087)
- SOYBEAN OIL (UNII: 241ATL177A)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DEXPANTHENOL (UNII: 1O6C93RI7Z)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SORBITOL (UNII: 506T60A25R)
- RICINOLEIC ACID (UNII: I2D0F69854)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- SQUALANE (UNII: GW89575KF9)
- .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
- CARRAGEENAN (UNII: 5C69YCD2YJ)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- TRITICUM AESTIVUM POLLEN (UNII: F1KAH8374D)
- CAT'S CLAW (UNII: 9060PRM18Q)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
What is the NDC to RxNorm Crosswalk for Inflammation Otc Radiation Relief?
- RxCUI: 1087954 - allantoin 0.5 % Topical Lotion
- RxCUI: 1087954 - allantoin 5 MG/ML Topical Lotion
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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".