NDC 63148-241 Antimicrobial Foaming Falling Rain
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63148 - Apollo Health And Beauty Care
- 63148-241 - Antimicrobial Foaming
Product Packages
NDC Code 63148-241-12
Package Description: 354 mL in 1 BOTTLE
Product Details
What is NDC 63148-241?
What are the uses for Antimicrobial Foaming Falling Rain?
Which are Antimicrobial Foaming Falling Rain UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (Active Moiety)
Which are Antimicrobial Foaming Falling Rain 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)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCERIN (UNII: PDC6A3C0OX)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- GINGER (UNII: C5529G5JPQ)
- HIBISCUS SABDARIFFA FLOWER (UNII: 45TGG6IU6M)
- CHAMOMILE (UNII: FGL3685T2X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- OREGANO (UNII: 0E5AT8T16U)
- THYME (UNII: CW657OBU4N)
- CINNAMON BARK OIL (UNII: XE54U569EC)
- ROSEMARY (UNII: IJ67X351P9)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- EDETATE SODIUM (UNII: MP1J8420LU)
- D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Antimicrobial Foaming Falling Rain?
- RxCUI: 1053207 - benzethonium chloride 0.1 % Medicated Liquid Soap
- RxCUI: 1053207 - benzethonium chloride 1 MG/ML Medicated Liquid Soap
* 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".