NDC 0363-9006 Walgreens Hand Sanitizer Coastal Breeze Scent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0363 - Walgreen Company
- 0363-9006 - Walgreens Hand Sanitizer Coastal Breeze Scent
Product Packages
NDC Code 0363-9006-01
Package Description: 59 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 0363-9006?
What are the uses for Walgreens Hand Sanitizer Coastal Breeze Scent?
Which are Walgreens Hand Sanitizer Coastal Breeze Scent UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Walgreens Hand Sanitizer Coastal Breeze Scent 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)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- .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 Walgreens Hand Sanitizer Coastal Breeze Scent?
- RxCUI: 2287763 - ethanol 69 % Topical Gel
- RxCUI: 2287763 - ethanol 0.69 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".