NDC 61543-0000 Porcelana 24 Hour Skin Lightening
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 61543-0000?
What are the uses for Porcelana 24 Hour Skin Lightening?
Which are Porcelana 24 Hour Skin Lightening UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROQUINONE (UNII: XV74C1N1AE)
- HYDROQUINONE (UNII: XV74C1N1AE) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Porcelana 24 Hour Skin Lightening 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)
- MINERAL OIL (UNII: T5L8T28FGP)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- BETA CAROTENE (UNII: 01YAE03M7J)
- MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
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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".