NDC 49371-047 Aromafields Tiger Lily Scented Anti-bacterial Hand
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49371 - Alily (zhangzhou) Bath Products Ltd.
- 49371-047 - Aromafields Tiger Lily Scented Anti-bacterial Hand
Product Packages
NDC Code 49371-047-01
Package Description: 500 g in 1 BOTTLE
Product Details
What is NDC 49371-047?
What are the uses for Aromafields Tiger Lily Scented Anti-bacterial Hand?
Which are Aromafields Tiger Lily Scented Anti-bacterial Hand UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Aromafields Tiger Lily Scented Anti-bacterial Hand 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)
- TROLAMINE (UNII: 9O3K93S3TK)
- MINERAL OIL (UNII: T5L8T28FGP)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PETROLATUM (UNII: 4T6H12BN9U)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CETEARETH-30 (UNII: 1R9DCZ5FOX)
- CETEARETH-12 (UNII: 7V4MR24V5P)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CARBOMER HOMOPOLYMER TYPE A (UNII: F68VH75CJC)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
What is the NDC to RxNorm Crosswalk for Aromafields Tiger Lily Scented Anti-bacterial Hand?
- RxCUI: 1047939 - triclosan 0.15 % Topical Lotion
- RxCUI: 1047939 - triclosan 1.5 MG/ML Topical Lotion
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[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".