NDC 11697-462 Forever Sun Lips
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11697 - Aloe Vera Of America, Inc.
- 11697-462 - Forever Sun Lips
Product Packages
NDC Code 11697-462-03
Package Description: 12 CARTON in 1 BOX / 1 TUBE in 1 CARTON (11697-462-02) / 4.25 g in 1 TUBE (11697-462-01)
Product Details
What is NDC 11697-462?
What are the uses for Forever Sun Lips?
Which are Forever Sun Lips UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Forever Sun Lips 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:
- SOYBEAN OIL (UNII: 241ATL177A)
- CERESIN (UNII: Q1LS2UJO3A)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- ETHYLHEXYL HYDROXYSTEARATE (UNII: B7I80BVV5E)
- CANDELILLA WAX (UNII: WL0328HX19)
- JOJOBA OIL (UNII: 724GKU717M)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALLANTOIN (UNII: 344S277G0Z)
* Please review the disclaimer below.
[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".