NDC 49035-440 Equate Beauty Color Safe Dandruff Conditioner
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49035 - Wal-mart Store Inc
- 49035-440 - Equate Beauty Color Safe Dandruff Conditioner
Product Packages
NDC Code 49035-440-14
Package Description: 420 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 49035-440?
What are the uses for Equate Beauty Color Safe Dandruff Conditioner?
Which are Equate Beauty Color Safe Dandruff Conditioner 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 Conditioner 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)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- COCONUT OIL (UNII: Q9L0O73W7L)
- PPG-3 BENZYL ETHER ETHYLHEXANOATE (UNII: 3N703GY99W)
- LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX)
- HYDROXYETHYL CELLULOSE (5000 CPS AT 1%) (UNII: X70SE62ZAR)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
What is the NDC to RxNorm Crosswalk for Equate Beauty Color Safe Dandruff Conditioner?
- RxCUI: 1052932 - zinc pyrithione 0.3 % Medicated Shampoo
- RxCUI: 1052932 - zinc pyrithione 3 MG/ML Medicated Shampoo
* 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".