NDC 77879-006 Lfg
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77879 - Bt Supplies West Inc
- 77879-006 - Lfg
Product Packages
NDC Code 77879-006-00
Package Description: 473 mL in 1 BOTTLE
Product Details
What is NDC 77879-006?
What are the uses for Lfg?
Which are Lfg UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- CHLOROXYLENOL (UNII: 0F32U78V2Q) (Active Moiety)
Which are Lfg 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 LAURETH SULFATE (UNII: BPV390UAP0)
- COCOYL METHYL MONOETHANOLAMINE (UNII: 79G1T427CF)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ALCOHOL (UNII: 3K9958V90M)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- MAGNESIUM NITRATE (UNII: 77CBG3UN78)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
What is the NDC to RxNorm Crosswalk for Lfg?
- RxCUI: 413261 - chloroxylenol 0.3 % Medicated Liquid Soap
- RxCUI: 413261 - chloroxylenol 3 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".