NDC 76144-237 Paulas Choice On-the-go Shielding Powder Broad Spectrum Spf 30
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What is NDC 76144-237?
What are the uses for Paulas Choice On-the-go Shielding Powder Broad Spectrum Spf 30?
Which are Paulas Choice On-the-go Shielding Powder Broad Spectrum Spf 30 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 Paulas Choice On-the-go Shielding Powder Broad Spectrum Spf 30 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:
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ORYZA SATIVA WHOLE (UNII: 84IVV0906Z)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- WATER (UNII: 059QF0KO0R)
- SALIX NIGRA BARK (UNII: QU52J3A5B3)
- EDETIC ACID (UNII: 9G34HU7RV0)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- BORON NITRIDE (UNII: 2U4T60A6YD)
- VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- NYLON 612 CYCLIC DIMER (UNII: Q1D37SUG0G)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CERAMIDE NP (UNII: 4370DF050B)
- STEARIC ACID (UNII: 4ELV7Z65AP)
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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".