NDC 75063-0015 Rainbow Hand Sanitizer Red
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75063 - Belleson Inc
- 75063-0015 - Rainbow Hand Sanitizer Red
Product Packages
NDC Code 75063-0015-1
Package Description: 500 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 75063-0015?
What are the uses for Rainbow Hand Sanitizer Red?
Which are Rainbow Hand Sanitizer Red UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Rainbow Hand Sanitizer Red 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- MORUS ALBA ROOT (UNII: CST1G9BZGD)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- TROLAMINE (UNII: 9O3K93S3TK)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- CAMELLIA SINENSIS ROOT (UNII: 8H54O0V2K3)
- LICORICE (UNII: 61ZBX54883)
- ROSEMARY (UNII: IJ67X351P9)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)
What is the NDC to RxNorm Crosswalk for Rainbow Hand Sanitizer Red?
- 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".