Label: CICA REDNESS SOLUTION SUNSCREEN- zinc oxide cream
- NDC Code(s): 73877-006-01, 73877-006-02
- Packager: Meebak Beauty, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 18, 2025
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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DOSAGE & ADMINISTRATION
For sunscreen use:
- Apply liberally 15 minutes before sun exposure
- Reapply at least every two hours
- Use a water-resistant sunscreen if swimming or sweating
- Sun protection measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and other sun protection measures including: 1) Limit time in the sun, especially from 10 a.m. to 2 p.m. 2) Wear long-sleeved shirts, pants, hats, and sunglasses
- Children under 6 months of age: Ask a doctor. - WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENT
WATER, CYCLOPENTASILOXANE, BUTYLENE GLYCOL, ISODODECANE, BUTYLOCTYL SALICYLATE, TITANIUM DIOXIDE (CI 77891), TRIMETHYLSILOXYSILICATE, CAPRYLYL METHICONE, LAURYL PEG-10 TRIS(TRIMETHYLSILOXY) SILYLETHYL DIMETHICONE, BUTYLENE GLYCOL, DICAPRYLATE/DICAPRATE, SYNTHETIC FLUORPHLOGOPITE, TRIDECYL TRIMELLITATE, PENTYLENE GLYCOL, DISTEARDIMONIUM HECTORITE, MAGNESIUM SULFATE, LAURYL PEG-8 DIMETHICONE, IRON OXIDES(CI 77492), TRIETHOXYCAPRYLYLSILANE, CAPRYLYL GLYCOL, GLYCERYL CAPRYLATE, CHROMIUM OXIDE GREENS, IRON OXIDES(CI 77491), ZEIN, IRON OXIDES(CI 77499), ETHYLHEXYLGLYCERIN, ALUMINUM HYDROXIDE, SILICA, DIMETHYL SILYLATE, FRAGRANCE, ZEA MAYS (CORN) STARCH, HYDROGENATED LECITHIN, CAPRYLIC/CAPRIC TRIGLYCERIDE, GLYCERIN, TOCOPHEROL, NELUMBO NUCIFERA FLOWER WATER, 1,2-HEXANEDIOL, CENTELLA ASIATICA EXTRACT, FICUS CARICA (FIG) FRUIT EXTRACT, INONOTUS OBLIQUUS (MUSHROOM) EXTRACT, CALENDULA OFFICINALIS FLOWER EXTRACT, TARAXACUM OFFICINALE (DANDELION) LEAF EXTRACT, MICROCITRUS AUSTRALASICA FRUIT EXTRACT, CERAMIDE NP
- OTHER SAFETY INFORMATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CICA REDNESS SOLUTION SUNSCREEN
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73877-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 170 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOPENTASILOXANE (UNII: 0THT5PCI0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) ISODODECANE (UNII: A8289P68Y2) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI) MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M) TRIDECYL TRIMELLITATE (UNII: FY36J270ES) PENTYLENE GLYCOL (UNII: 50C1307PZG) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) LAURYL PEG-8 DIMETHICONE (300 CPS) (UNII: ELL2U7K8T8) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) CAPRYLYL GLYCOL (UNII: 00YIU5438U) GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A) CHROMIC OXIDE (UNII: X5Z09SU859) FERRIC OXIDE RED (UNII: 1K09F3G675) ZEIN (UNII: 80N308T1NN) FERROSOFERRIC OXIDE (UNII: XM0M87F357) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) STARCH, CORN (UNII: O8232NY3SJ) HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) GLYCERIN (UNII: PDC6A3C0OX) TOCOPHEROL (UNII: R0ZB2556P8) NELUMBO NUCIFERA FLOWER OIL (UNII: P658Q19EG2) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J) FIG (UNII: TGD87RII2U) INONOTUS OBLIQUUS FRUITING BODY (UNII: MRO1FS760M) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) TARAXACUM OFFICINALE LEAF (UNII: 0022LFJ74Y) CITRUS AUSTRALASICA WHOLE (UNII: NS4TX5KDU5) CERAMIDE NP (UNII: 4370DF050B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73877-006-02 1 in 1 CARTON 08/12/2025 1 NDC:73877-006-01 50 mL in 1 TUBE; 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 08/12/2025 Labeler - Meebak Beauty, Inc (695798521) Registrant - Meebak Beauty, Inc (695798521) Establishment Name Address ID/FEI Business Operations Kolmar Korea Co., Ltd 963271745 manufacture(73877-006)
