NDC 30142-079 Kroger Waterless Hand Sanitizer With Aloe
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 30142 - The Kroger Company
- 30142-079 - Kroger
Product Packages
NDC Code 30142-079-02
Package Description: 59 mL in 1 BOTTLE, PLASTIC
NDC Code 30142-079-08
Package Description: 236 mL in 1 BOTTLE, PLASTIC
NDC Code 30142-079-09
Package Description: 236 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 30142-079?
What are the uses for Kroger Waterless Hand Sanitizer With Aloe?
Which are Kroger Waterless Hand Sanitizer With Aloe UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Kroger Waterless Hand Sanitizer With Aloe 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)
- CARBOMER 934 (UNII: Z135WT9208)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Kroger Waterless Hand Sanitizer With Aloe?
- RxCUI: 582753 - ethanol 70 % Topical Solution
- RxCUI: 582753 - ethanol 0.7 ML/ML Topical Solution
- RxCUI: 582753 - ethyl alcohol 70 % Topical Solution
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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".