NDC 58666-3412 African Black Facial Cleansing Bar Anti-acne Clarifying
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58666 - Sundial Group Llc
- 58666-3412 - African Black Facial Cleansing Bar Anti-acne Clarifying
Product Packages
NDC Code 58666-3412-7
Package Description: 99 g in 1 BOX
Product Details
What is NDC 58666-3412?
What are the uses for African Black Facial Cleansing Bar Anti-acne Clarifying?
Which are African Black Facial Cleansing Bar Anti-acne Clarifying UNII Codes?
The UNII codes for the active ingredients in this product are:
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- CENTELLA ASIATICA (UNII: 7M867G6T1U) (Active Moiety)
- MELISSA OFFICINALIS (UNII: YF70189L0N)
- MELISSA OFFICINALIS (UNII: YF70189L0N) (Active Moiety)
- ALOE (UNII: V5VD430YW9)
- ALOE (UNII: V5VD430YW9) (Active Moiety)
Which are African Black Facial Cleansing Bar Anti-acne Clarifying 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:
- SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- SHEA BUTTER (UNII: K49155WL9Y)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- OATMEAL (UNII: 8PI54V663Y)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- TEA TREE OIL (UNII: VIF565UC2G)
- SODIUM GLUCONATE (UNII: R6Q3791S76)
- SODIUM PALMATE (UNII: S0A6004K3Z)
- ALCOHOL (UNII: 3K9958V90M)
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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".