NDC 0363-9005 Walgreens Advanced Hand Sanitizer Made With Plant-based Ethyl Alcohol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0363 - Walgreen Company
- 0363-9005 - Walgreens Advanced Hand Sanitizer Made With Plant-based Ethyl Alcohol
Product Packages
NDC Code 0363-9005-01
Package Description: 236 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 0363-9005?
What are the uses for Walgreens Advanced Hand Sanitizer Made With Plant-based Ethyl Alcohol?
Which are Walgreens Advanced Hand Sanitizer Made With Plant-based Ethyl Alcohol UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Walgreens Advanced Hand Sanitizer Made With Plant-based Ethyl Alcohol 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:
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- LITSEA OIL (UNII: 2XIW34BN6O)
- POGOSTEMON CABLIN LEAF OIL (UNII: F3IN55X5PO)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- MANDARIN OIL (UNII: NJO720F72R)
What is the NDC to RxNorm Crosswalk for Walgreens Advanced Hand Sanitizer Made With Plant-based Ethyl Alcohol?
- RxCUI: 2287763 - ethanol 69 % Topical Gel
- RxCUI: 2287763 - ethanol 0.69 ML/ML Topical Gel
* 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".