NDC 58503-064 Xtracare 2 In 1 Hair Cleanse And Condition Coconut Water
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58503 - China Ningbo Shangge Cosmetic Technology Corp.
- 58503-064 - Xtracare 2 In 1 Hair Cleanse And Condition
Product Packages
NDC Code 58503-064-01
Package Description: 400 g in 1 BOTTLE
Product Details
What is NDC 58503-064?
What are the uses for Xtracare 2 In 1 Hair Cleanse And Condition Coconut Water?
Which are Xtracare 2 In 1 Hair Cleanse And Condition Coconut Water 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 Xtracare 2 In 1 Hair Cleanse And Condition Coconut Water 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)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- GLYCERIN (UNII: PDC6A3C0OX)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
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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".