Label: (S)UNDERCOVER SPF 50- zinc oxide lotion
- NDC Code(s): 73088-106-12
- Packager: TUBBY TODD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 23, 2024
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- ACTIVE INGREDIENTS
- PURPOSE
- USES
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
-
DIRECTIONS
- Apply generously 15 minutes before sun exposure and as needed.
- Reapply
- after 40 minutes of swimming or sweating
- immediately after towel drying
- at least every 2 hours
- Children under 6 months of age: ask a doctor.
- 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:
- limit time in the sun, especially from 10am-2pm
- wear long-sleeved shirts, pants, hats, and sunglasses.
- OTHER INFORMATION
-
INACTIVE INGREDIENT
Allantoin, Bisabolol, C12-15 Alkyl Benzoate, Caprylic/Capric Triglyceride, Caprylyl Glycol, Coco-Caprylate, Helianthus Annuus (Sunflower) Extract, Jojoba Esters, Lecithin, Methylpropanediol, Niacinamide, Nylon-12, Orza Sativa (Rice) Bran Extract, Phenylpropanol, Polyglyceryl-2 Dipolyhydroxystearate, Polyglyceryl-3 Diisostearate, Polyglyceryl-3 Polyricinoleate, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Propanediol, Rosmarinus Officinalis (Rosemary) Leaf Extract, Silica, Sodium Chloride, Sodium Hydroxide, Stearalkonium Hectorite, Tetrasodium Glutamate Diacetate, Tocopherol, Tridecyl Salicylate, Water
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
(S)UNDERCOVER SPF 50
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73088-106 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 12 g in 100 mL Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) HYDROLYZED JOJOBA ESTERS (UNII: UDR641JW8W) SODIUM HYDROXIDE (UNII: 55X04QC32I) TOCOPHEROL (UNII: R0ZB2556P8) WATER (UNII: 059QF0KO0R) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) CAPRYLYL GLYCOL (UNII: 00YIU5438U) COCO-CAPRYLATE (UNII: 4828G836N6) HELIANTHUS ANNUUS WHOLE (UNII: 17S27ZT6KR) HYDROGENATED JOJOBA OIL/JOJOBA OIL, RANDOMIZED (IODINE VALUE 40-44) (UNII: AS2SZ9757N) LECITHIN, SUNFLOWER (UNII: 834K0WOS5G) PHENYLPROPANOL (UNII: 0F897O3O4M) POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12) POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y) PROPANEDIOL (UNII: 5965N8W85T) ROSMARINUS OFFICINALIS WHOLE (UNII: EA3289138M) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM CHLORIDE (UNII: 451W47IQ8X) TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) NYLON-12 (UNII: 446U8J075B) RICE BRAN (UNII: R60QEP13IC) BISABOLOL (UNII: 24WE03BX2T) NIACINAMIDE (UNII: 25X51I8RD4) TRIDECYL SALICYLATE (UNII: AZQ08K38Z1) POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4) METHYLPROPANEDIOL (UNII: N8F53B3R4R) STEARALKONIUM HECTORITE (UNII: OLX698AH5P) POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73088-106-12 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/14/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 04/14/2022 Labeler - TUBBY TODD (052545299)
