NDC 73932-0017 Clean Care Fresh Hand Sanitizer (ethanol Gel)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73932 - At Bio Pharm Co Ltd
- 73932-0017 - Clean Care Fresh Hand Sanitizer (ethanol Gel)
Product Packages
NDC Code 73932-0017-1
Package Description: 500 mL in 1 BOTTLE
NDC Code 73932-0017-2
Package Description: 3785 mL in 1 BOTTLE
Product Details
What is NDC 73932-0017?
What are the uses for Clean Care Fresh Hand Sanitizer (ethanol Gel)?
Which are Clean Care Fresh Hand Sanitizer (ethanol Gel) UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Clean Care Fresh Hand Sanitizer (ethanol Gel) 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:
- ROSEMARY OIL (UNII: 8LGU7VM393)
- PAEONIA SUFFRUTICOSA ROOT BARK (UNII: BUG255FE7X)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
What is the NDC to RxNorm Crosswalk for Clean Care Fresh Hand Sanitizer (ethanol Gel)?
- RxCUI: 1305100 - ethanol 75 % Topical Gel
- RxCUI: 1305100 - ethanol 0.75 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".