NDC 75063-0007 Rainbow Hand Sanitizer Pink
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75063 - Belleson Inc
- 75063-0007 - Rainbow Hand Sanitizer Pink
Product Packages
NDC Code 75063-0007-1
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 40 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 75063-0007?
What are the uses for Rainbow Hand Sanitizer Pink?
Which are Rainbow Hand Sanitizer Pink 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 Pink 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)
- ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- MORUS ALBA ROOT (UNII: CST1G9BZGD)
- LICORICE (UNII: 61ZBX54883)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
What is the NDC to RxNorm Crosswalk for Rainbow Hand Sanitizer Pink?
- RxCUI: 1812262 - ethanol 68 % Topical Spray
- RxCUI: 1812262 - ethanol 0.68 ML/ML Topical Spray
* 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".