NDC 62673-016 Zincon Medicated Dandruff
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 62673-016?
What are the uses for Zincon Medicated Dandruff?
Which are Zincon Medicated 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 Zincon Medicated 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- WATER (UNII: 059QF0KO0R)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
What is the NDC to RxNorm Crosswalk for Zincon Medicated Dandruff?
- RxCUI: 1246250 - Zincon Dandruff 1 % Medicated Shampoo
- RxCUI: 1246250 - zinc pyrithione 10 MG/ML Medicated Shampoo [Zincon]
- RxCUI: 1246250 - Zincon 10 MG/ML Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 10 MG/ML Medicated 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".