NDC 62032-102 Nu-derm Physical Uv Block Spf 32
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62032 - Omp, Inc.
- 62032-102 - Nu-derm Physical Uv Block
Product Characteristics
Product Packages
NDC Code 62032-102-36
Package Description: 57 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 62032-102?
What are the uses for Nu-derm Physical Uv Block Spf 32?
Which are Nu-derm Physical Uv Block Spf 32 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Nu-derm Physical Uv Block Spf 32 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:
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- WATER (UNII: 059QF0KO0R)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- GLYCERETH-26 (UNII: NNE56F2N14)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
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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".