NDC 49035-437 Equate Beauty Color Safe Dandruff
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49035 - Wal-mart Store Inc
- 49035-437 - Equate Beauty Color Safe Dandruff
Product Packages
NDC Code 49035-437-14
Package Description: 420 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 49035-437?
What are the uses for Equate Beauty Color Safe Dandruff?
Which are Equate Beauty Color Safe Dandruff UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- PYRITHIONE ZINC (UNII: R953O2RHZ5) (Active Moiety)
Which are Equate Beauty Color Safe Dandruff 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)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ALMOND OIL (UNII: 66YXD4DKO9)
- QUATERNIUM-22 (UNII: MXO138JCBP)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- AMODIMETHICONE (3500 CST) (UNII: 42AFE8JAOY)
- POLIDOCANOL (UNII: 0AWH8BFG9A)
- GLYCERIN (UNII: PDC6A3C0OX)
- TRIDECETH-12 (UNII: YFY3KG5Y7O)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
What is the NDC to RxNorm Crosswalk for Equate Beauty Color Safe Dandruff?
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 10 MG/ML Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Conditioner
* 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".