NDC 49035-918 Equate Clinical Strength Dandruff
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49035 - Wal-mart Stores Inc
- 49035-918 - Equate
Product Packages
NDC Code 49035-918-14
Package Description: 420 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 49035-918?
What are the uses for Equate Clinical Strength Dandruff?
Which are Equate Clinical Strength Dandruff UNII Codes?
The UNII codes for the active ingredients in this product are:
- SELENIUM SULFIDE (UNII: Z69D9E381Q)
- SELENIUM SULFIDE (UNII: Z69D9E381Q) (Active Moiety)
Which are Equate Clinical Strength 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)
- AMMONIUM LAURETH-3 SULFATE (UNII: 896SJ235FN)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
What is the NDC to RxNorm Crosswalk for Equate Clinical Strength Dandruff?
- RxCUI: 204642 - selenium sulfide 1 % Medicated Shampoo
- RxCUI: 204642 - selenium sulfide 10 MG/ML Medicated Shampoo
- RxCUI: 204642 - selenium sulfide 1 % Lotion Shampoo
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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".