NDC 59779-224 Instant Hand Sanitizer With Shea Butter
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs Pharmacy
- 59779-224 - Instant Hand Sanitizer
Product Packages
NDC Code 59779-224-01
Package Description: 15 mL in 1 BOTTLE
NDC Code 59779-224-02
Package Description: 59 mL in 1 BOTTLE
NDC Code 59779-224-08
Package Description: 236 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 59779-224?
What are the uses for Instant Hand Sanitizer With Shea Butter?
Which are Instant Hand Sanitizer With Shea Butter UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Instant Hand Sanitizer With Shea Butter 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, D- (UNII: A7E6112E4N)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- SHEA BUTTER (UNII: K49155WL9Y)
- MANNITOL (UNII: 3OWL53L36A)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- CARBOMER 934 (UNII: Z135WT9208)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Instant Hand Sanitizer With Shea Butter?
- 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".