Label: (S)UNDERCOVER SPF 50- zinc oxide lotion
- NDC Code(s): 73088-106-12
- Packager: TUBBY TODD
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 12, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- PURPOSE
- USES
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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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, METHYLHEPTYL ISOSTEARATE, METHYLPROPANEDIOL, NIACINAMIDE, NYLON-12, ORYZA SATIVA (RICE) BRAN EXTRACT, PHENYLPROPANOL, POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE, POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE, PROPANEDIOL, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT, SILICA, SODIUM CHLORIDE, TETRASODIUM GLUTAMATE DIACETATE, TRIDECYL SALICYLATE, TOCOPHEROL, 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 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) METHYLHEPTYL ISOSTEARATE (UNII: 981F40Q9FF) 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) .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z) NIACINAMIDE (UNII: 25X51I8RD4) TRIDECYL SALICYLATE (UNII: AZQ08K38Z1) 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)
