NDC 70112-300 Topicare Therapeutics Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70112 - Topicare Management, Llc
- 70112-300 - Topicare Therapeutics Hand Sanitizer
Product Packages
NDC Code 70112-300-01
Package Description: 3790 mL in 1 JUG
NDC Code 70112-300-02
Package Description: 59 mL in 1 BOTTLE
NDC Code 70112-300-04
Package Description: 118 mL in 1 BOTTLE
NDC Code 70112-300-08
Package Description: 236 mL in 1 BOTTLE
NDC Code 70112-300-16
Package Description: 473 mL in 1 BOTTLE
Product Details
What is NDC 70112-300?
What are the uses for Topicare Therapeutics Hand Sanitizer?
Which are Topicare Therapeutics Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Topicare Therapeutics Hand Sanitizer 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- MYRISTYL LACTATE (UNII: 1D822OC34X)
- LAURYL LACTATE (UNII: G5SU0BFK7O)
- HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
- CETYL LACTATE (UNII: A7EVH2RK4O)
What is the NDC to RxNorm Crosswalk for Topicare Therapeutics Hand Sanitizer?
- RxCUI: 2288239 - ethanol 73.3 % Topical Gel
- RxCUI: 2288239 - ethanol 0.733 ML/ML 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".