NDC 78565-007 Zinc
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78565 - Meixin Beauty & Health Care Products Co., Ltd.
- 78565-007 - Zinc
Product Characteristics
Product Packages
NDC Code 78565-007-02
Package Description: 240 g in 1 BOX
Product Details
What is NDC 78565-007?
What are the uses for Zinc?
Which are Zinc 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 Zinc 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:
- EDETATE SODIUM (UNII: MP1J8420LU)
- SODIUM PALMITATE (UNII: JQ43KP6296)
- SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Zinc?
- RxCUI: 283707 - zinc pyrithione 2 % Medicated Bar Soap
- RxCUI: 283707 - zinc pyrithione 0.02 MG/MG Medicated Bar Soap
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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".