NDC 68828-199 Skin Brightening Antiperspirant Deodorant Roll-on Jafra Daily
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 68828-199?
What are the uses for Skin Brightening Antiperspirant Deodorant Roll-on Jafra Daily?
Which are Skin Brightening Antiperspirant Deodorant Roll-on Jafra Daily UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M)
- ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (Active Moiety)
Which are Skin Brightening Antiperspirant Deodorant Roll-on Jafra Daily 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)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PEG-25 PROPYLENE GLYCOL STEARATE (UNII: X21KPH4633)
- GLYCOL STEARATE (UNII: 0324G66D0E)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- AZADIRACHTA INDICA BARK (UNII: G580B439YI)
- TURMERIC (UNII: 856YO1Z64F)
- HEMIDESMUS INDICUS ROOT (UNII: Y5CFT48S90)
- SPHAERANTHUS INDICUS FLOWERING TOP (UNII: 1O5Y93LB44)
- PHYLLANTHUS EMBLICA FRUIT (UNII: YLX4CW2576)
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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".