NDC 82343-010 Dr. Scalp Active
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 82343 - Dr Scalp Co., Ltd.
- 82343-010 - Dr. Scalp Active
Product Packages
NDC Code 82343-010-02
Package Description: 1 BOTTLE, PUMP in 1 CARTON / 500 g in 1 BOTTLE, PUMP (82343-010-01)
Product Details
What is NDC 82343-010?
What are the uses for Dr. Scalp Active?
Which are Dr. Scalp Active 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 Dr. Scalp Active 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 C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
What is the NDC to RxNorm Crosswalk for Dr. Scalp Active?
- RxCUI: 1245937 - zinc pyrithione 0.48 % Topical Gel
- RxCUI: 1245937 - zinc pyrithione 4.8 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".