NDC 62839-0271 Nu Skin Antibacterial Body Cleansing
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62839 - Nse Products, Inc.
- 62839-0271 - Nu Skin
Product Packages
NDC Code 62839-0271-8
Package Description: 250 mL in 1 BOTTLE, PLASTIC
NDC Code 62839-0271-9
Package Description: 500 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 62839-0271?
What are the uses for Nu Skin Antibacterial Body Cleansing?
Which are Nu Skin Antibacterial Body Cleansing UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Nu Skin Antibacterial Body Cleansing 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)
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GRAPEFRUIT (UNII: O82C39RR8C)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- SODIUM COPPER CHLOROPHYLLIN (UNII: 1D276TYV9O)
What is the NDC to RxNorm Crosswalk for Nu Skin Antibacterial Body Cleansing?
- RxCUI: 1050670 - triclosan 0.55 % Medicated Liquid Soap
- RxCUI: 1050670 - triclosan 5.5 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".