NDC 64942-1302 Axe 2 In 1 Armor Antidandruff 2 In 1
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 64942-1302-1
Package Description: 650 mL in 1 CONTAINER
NDC Code 64942-1302-2
Package Description: 355 mL in 1 CONTAINER
NDC Code 64942-1302-3
Package Description: 443 mL in 1 CONTAINER
NDC Code 64942-1302-4
Package Description: 50 mL in 1 CONTAINER
Product Details
What is NDC 64942-1302?
What are the uses for Axe 2 In 1 Armor Antidandruff 2 In 1?
Which are Axe 2 In 1 Armor Antidandruff 2 In 1 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 Axe 2 In 1 Armor Antidandruff 2 In 1 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)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- TRIETHANOLAMINE DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)
- 1,3-BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- PPG-9 (UNII: I29VQH0G0B)
What is the NDC to RxNorm Crosswalk for Axe 2 In 1 Armor Antidandruff 2 In 1?
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 10 MG/ML Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Conditioner
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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".