NDC 74721-0020 Safe Cleaner Plus
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 74721 - S-one Pharmaceutical Inc
- 74721-0020 - Safe Cleaner Plus
Product Packages
NDC Code 74721-0020-0
Package Description: 60 mL in 1 BOTTLE
NDC Code 74721-0020-1
Package Description: 500 mL in 1 BOTTLE
NDC Code 74721-0020-2
Package Description: 2 mL in 1 POUCH
NDC Code 74721-0020-5
Package Description: 250 mL in 1 BOTTLE
NDC Code 74721-0020-6
Package Description: 475 mL in 1 BOTTLE
NDC Code 74721-0020-7
Package Description: 1000 mL in 1 BOTTLE
NDC Code 74721-0020-8
Package Description: 2000 mL in 1 BOTTLE
NDC Code 74721-0020-9
Package Description: 4000 mL in 1 BOTTLE
Product Details
What is NDC 74721-0020?
What are the uses for Safe Cleaner Plus?
Which are Safe Cleaner Plus UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Safe Cleaner Plus 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:
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- TROLAMINE (UNII: 9O3K93S3TK)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- CITRUS PARADISI SEED (UNII: 12F08874Y7)
What is the NDC to RxNorm Crosswalk for Safe Cleaner Plus?
- 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".