NDC 81711-001 Green F5 Sanitizing Hand Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81711 - Superman.co.,ltd
- 81711-001 - Green F5 Sanitizing Hand Wipes
Product Packages
NDC Code 81711-001-01
Package Description: 5000 g in 1 POUCH
Product Details
What is NDC 81711-001?
What are the uses for Green F5 Sanitizing Hand Wipes?
Which are Green F5 Sanitizing Hand Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Green F5 Sanitizing Hand Wipes 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)
- TROMETHAMINE (UNII: 023C2WHX2V)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
What is the NDC to RxNorm Crosswalk for Green F5 Sanitizing Hand Wipes?
- RxCUI: 1041780 - ethanol 62 % Medicated Pad
- RxCUI: 1041780 - ethanol 0.62 ML/ML Medicated Pad
- RxCUI: 1041780 - ethanol 62 % Hand Sanitizer Wipes
- RxCUI: 1041780 - ethanol 62 % Topical Cloth
- RxCUI: 1041780 - ethanol 62 % Topical Swab
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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".