NDC 75615-0040 Dr.homes Hand Clean
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75615 - Ui Cosmetics Co., Ltd
- 75615-0040 - Dr.homes Hand Clean
Product Packages
NDC Code 75615-0040-1
Package Description: 50 mL in 1 BOTTLE
NDC Code 75615-0040-2
Package Description: 60 mL in 1 BOTTLE
NDC Code 75615-0040-3
Package Description: 100 mL in 1 BOTTLE
NDC Code 75615-0040-4
Package Description: 200 mL in 1 BOTTLE, PUMP
NDC Code 75615-0040-5
Package Description: 250 mL in 1 BOTTLE, PUMP
NDC Code 75615-0040-6
Package Description: 300 mL in 1 BOTTLE, PUMP
NDC Code 75615-0040-7
Package Description: 500 mL in 1 BOTTLE, PUMP
NDC Code 75615-0040-8
Package Description: 5000 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 75615-0040?
What are the uses for Dr.homes Hand Clean?
Which are Dr.homes Hand Clean UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Dr.homes Hand Clean 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:
- TROLAMINE (UNII: 9O3K93S3TK)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
What is the NDC to RxNorm Crosswalk for Dr.homes Hand Clean?
- 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".