NDC 33992-1061 Assured Instant Hand Sanitizer With Moisturizers Aloe Vera And Moisturizers
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33992 - Greenbrier International, Inc.
- 33992-1061 - Assured Instant Hand Sanitizer With Moisturizers Aloe Vera And Moisturizers
Product Packages
NDC Code 33992-1061-0
Package Description: 295 mL in 1 BOTTLE
NDC Code 33992-1061-1
Package Description: 237 mL in 1 BOTTLE
Product Details
What is NDC 33992-1061?
What are the uses for Assured Instant Hand Sanitizer With Moisturizers Aloe Vera And Moisturizers?
Which are Assured Instant Hand Sanitizer With Moisturizers Aloe Vera And Moisturizers UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Assured Instant Hand Sanitizer With Moisturizers Aloe Vera And Moisturizers 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)
- TROLAMINE (UNII: 9O3K93S3TK)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Assured Instant Hand Sanitizer With Moisturizers Aloe Vera And Moisturizers?
- 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".