NDC 63148-252 Cvs Pharmacy Foam Hand Sanitizer With Aloe
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63148 - Apollo Health And Beauty Care
- 63148-252 - Cvs Pharmacy
Product Packages
NDC Code 63148-252-02
Package Description: 50 mL in 1 BOTTLE, PLASTIC
NDC Code 63148-252-08
Package Description: 236 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 63148-252?
What are the uses for Cvs Pharmacy Foam Hand Sanitizer With Aloe?
Which are Cvs Pharmacy Foam Hand Sanitizer With Aloe UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Cvs Pharmacy Foam Hand Sanitizer With Aloe 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)
- GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- OCTISALATE (UNII: 4X49Y0596W)
- PROPYLENE OXIDE (UNII: Y4Y7NYD4BK)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- AVOBENZONE (UNII: G63QQF2NOX)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
What is the NDC to RxNorm Crosswalk for Cvs Pharmacy Foam Hand Sanitizer With Aloe?
- RxCUI: 616805 - ethanol 70 % Topical Foam
- RxCUI: 616805 - ethanol 0.7 ML/ML Topical Foam
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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".