NDC 75368-020 Celraum Forest Perfect Hand Cleaner
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75368 - U&d2 Co.,ltd.
- 75368-020 - Celraum Forest Perfect Hand Cleaner
Product Packages
NDC Code 75368-020-01
Package Description: 50 mL in 1 CARTON
NDC Code 75368-020-02
Package Description: 500 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 75368-020?
What are the uses for Celraum Forest Perfect Hand Cleaner?
Which are Celraum Forest Perfect Hand Cleaner UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Celraum Forest Perfect Hand Cleaner 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)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- GLYCERIN (UNII: PDC6A3C0OX)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- TROLAMINE (UNII: 9O3K93S3TK)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- PANTHENOL (UNII: WV9CM0O67Z)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GINGER (UNII: C5529G5JPQ)
- SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C)
- COPTIS JAPONICA ROOT (UNII: JH0SWT16D1)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ASIATICOSIDE (UNII: PKO39VY215)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
What is the NDC to RxNorm Crosswalk for Celraum Forest Perfect Hand Cleaner?
- RxCUI: 581660 - ethanol 62 % Topical Gel
- RxCUI: 581660 - ethanol 0.62 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".