NDC 59779-200 Cvs Pharmacy Instant Hand Sanitizer With Aloe And Vitamin E
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs Pharmacy
- 59779-200 - Cvs Pharmacy Instant Hand Sanitizer With Aloe And Vitamin E
Product Packages
NDC Code 59779-200-02
Package Description: 59 mL in 1 BOTTLE
NDC Code 59779-200-08
Package Description: 236 mL in 1 BOTTLE
Product Details
What is NDC 59779-200?
What are the uses for Cvs Pharmacy Instant Hand Sanitizer With Aloe And Vitamin E?
Which are Cvs Pharmacy Instant Hand Sanitizer With Aloe And Vitamin E 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 Instant Hand Sanitizer With Aloe And Vitamin E 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)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- GLYCERIN (UNII: PDC6A3C0OX)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Cvs Pharmacy Instant Hand Sanitizer With Aloe And Vitamin E?
- RxCUI: 902574 - ethanol 65 % Topical Gel
- RxCUI: 902574 - ethanol 0.65 ML/ML Topical Gel
- RxCUI: 902574 - ethyl alcohol 65 % 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".