NDC 63148-251 Cvs Pharmacy Anti-aging Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63148 - Apollo Health And Beauty Care
- 63148-251 - Cvs Pharmacy
Product Packages
NDC Code 63148-251-08
Package Description: 236 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 63148-251?
What are the uses for Cvs Pharmacy Anti-aging Hand Sanitizer?
Which are Cvs Pharmacy Anti-aging Hand Sanitizer 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 Anti-aging Hand Sanitizer 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- NIACINAMIDE (UNII: 25X51I8RD4)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- 2-AMINO-2-METHYL-1-PROPANOL (UNII: LU49E6626Q)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- ARGININE (UNII: 94ZLA3W45F)
- ASPARTIC ACID (UNII: 30KYC7MIAI)
- GLYCINE (UNII: TE7660XO1C)
- ALANINE (UNII: OF5P57N2ZX)
- SERINE (UNII: 452VLY9402)
- VALINE (UNII: HG18B9YRS7)
- PROLINE (UNII: 9DLQ4CIU6V)
- THREONINE (UNII: 2ZD004190S)
- ISOLEUCINE (UNII: 04Y7590D77)
- HISTIDINE (UNII: 4QD397987E)
- PHENYLALANINE (UNII: 47E5O17Y3R)
- MANNITOL (UNII: 3OWL53L36A)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
What is the NDC to RxNorm Crosswalk for Cvs Pharmacy Anti-aging Hand Sanitizer?
- RxCUI: 581660 - ethanol 62 % Topical Gel
- RxCUI: 581660 - ethanol 0.62 ML/ML Topical Gel
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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".