SUNSOLVE MD CORRECT AND FADE- zinc oxide lotion
Sunsolve MD Correct and Fade by
Drug Labeling and Warnings
Sunsolve MD Correct and Fade by is a Otc medication manufactured, distributed, or labeled by Sunsolve MD Inc, Nanophase Technologies Corporation. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- Sunsolve MD Correct and Fade
- Sunsolve MD Correct and Fade
- Sunsolve MD Correct and Fade
- Sunsolve MD Correct and Fade
- Sunsolve MD Correct and Fade
- Sunsolve MD Correct and Fade
- Sunsolve MD Correct and Fade
- Sunsolve MD Correct and Fade
- Sunsolve MD Correct and Fade
-
INGREDIENTS AND APPEARANCE
SUNSOLVE MD CORRECT AND FADE
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 84878-200 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 132 mg in 1 mL Inactive Ingredients Ingredient Name Strength FERROSOFERRIC OXIDE (UNII: XM0M87F357) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U) FERRIC OXIDE RED (UNII: 1K09F3G675) GLYCERIN (UNII: PDC6A3C0OX) TOCOPHEROL (UNII: R0ZB2556P8) GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT (UNII: 2788Z9758H) JOJOBA OIL (UNII: 724GKU717M) ORYZA SATIVA WHOLE (UNII: 84IVV0906Z) TRIDECYL SALICYLATE (UNII: AZQ08K38Z1) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CAPRYLYL GLYCOL (UNII: 00YIU5438U) COCO-CAPRYLATE (UNII: 4828G836N6) NYLON-12 (UNII: 446U8J075B) PHENYLPROPANOL (UNII: 0F897O3O4M) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) METHYLPROPANEDIOL (UNII: N8F53B3R4R) POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12) ALLANTOIN (UNII: 344S277G0Z) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O) .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) NIACINAMIDE (UNII: 25X51I8RD4) PROPANEDIOL (UNII: 5965N8W85T) TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) SODIUM CHLORIDE (UNII: 451W47IQ8X) POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y) STEARALKONIUM HECTORITE (UNII: OLX698AH5P) POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8) Product Characteristics Color brown Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 84878-200-02 1 in 1 CARTON 11/06/2024 1 NDC: 84878-200-01 48 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 11/06/2024 Labeler - Sunsolve MD Inc (119376976) Registrant - Nanophase Technologies Corporation (623502044) Establishment Name Address ID/FEI Business Operations Nanophase Technologies Corporation 050383046 api manufacture(84878-200) Establishment Name Address ID/FEI Business Operations Nanophase Technologies Corporation 118812921 pack(84878-200) , manufacture(84878-200) Establishment Name Address ID/FEI Business Operations Nanophase Technologies Corporation 623502044 api manufacture(84878-200) , manufacture(84878-200)
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.