NDC 42851-039 Zo Skin Health Pigment Control Plus Blending Creme Hydroquinone
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 42851-039?
What are the uses for Zo Skin Health Pigment Control Plus Blending Creme Hydroquinone?
Which are Zo Skin Health Pigment Control Plus Blending Creme Hydroquinone UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROQUINONE (UNII: XV74C1N1AE)
- HYDROQUINONE (UNII: XV74C1N1AE) (Active Moiety)
Which are Zo Skin Health Pigment Control Plus Blending Creme Hydroquinone 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)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- DIOSCOREA VILLOSA TUBER (UNII: IWY3IWX2G8)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- PALMITIC ACID (UNII: 2V16EO95H1)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- QUILLAJA SAPONARIA BARK (UNII: 8N0K3807ZW)
- SMILAX ARISTOLOCHIIFOLIA ROOT (UNII: NR100Y25G0)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- SODIUM SULFITE (UNII: VTK01UQK3G)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- YUCCA SCHIDIGERA ROOT (UNII: E2H9ET15AT)
What is the NDC to RxNorm Crosswalk for Zo Skin Health Pigment Control Plus Blending Creme Hydroquinone?
- RxCUI: 244594 - hydroquinone 2 % Topical Lotion
- RxCUI: 244594 - hydroquinone 20 MG/ML Topical Lotion
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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".