NDC 10967-672 Ea Eight Hour Skin Protectant
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10967 - Revlon
- 10967-672 - Ea Eight Hour Skin Protectant
Product Packages
NDC Code 10967-672-17
Package Description: 50 g in 1 TUBE
Product Details
What is NDC 10967-672?
What are the uses for Ea Eight Hour Skin Protectant?
Which are Ea Eight Hour Skin Protectant UNII Codes?
The UNII codes for the active ingredients in this product are:
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Ea Eight Hour Skin Protectant 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:
- CITRAL (UNII: T7EU0O9VPP)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- MINERAL OIL (UNII: T5L8T28FGP)
- SOYBEAN OIL (UNII: 241ATL177A)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- GERANIOL (UNII: L837108USY)
- CORN OIL (UNII: 8470G57WFM)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CASTOR OIL (UNII: D5340Y2I9G)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- TOCOPHEROL (UNII: R0ZB2556P8)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- LANOLIN (UNII: 7EV65EAW6H)
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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".