NDC 70416-2001 Care On Hand Sanitizer Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70416 - Welcron Healthcare Co., Ltd
- 70416-2001 - Care On Hand Sanitizer Gel
Product Packages
NDC Code 70416-2001-1
Package Description: 500 mL in 1 BOTTLE, PUMP
NDC Code 70416-2001-2
Package Description: 100 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 70416-2001?
What are the uses for Care On Hand Sanitizer Gel?
Which are Care On Hand Sanitizer Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Care On Hand Sanitizer 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:
- WATER (UNII: 059QF0KO0R)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- TROLAMINE (UNII: 9O3K93S3TK)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- LICORICE (UNII: 61ZBX54883)
- ROSEMARY (UNII: IJ67X351P9)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Care On Hand Sanitizer Gel?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % Topical Gel
* Please review the disclaimer below.
[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".