Label: COPPERTONE PURE AND SIMPLE KIDS SUNCREEN SPF 50- zinc oxide 24.08% lotion
- NDC Code(s): 66800-2744-6
- Packager: Beiersdorf Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 19, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Use
- Warnings
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
Directions
■ shake well before each use
■ apply liberally 15 minutes before sun exposure
■ reapply:
■ after 80 minutes of swimming or sweating
■ immediately after towel drying
■ at least every 2 hours
■ 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 10 a.m. – 2 p.m.
■ wear long-sleeve shirts, pants, hats, and sunglasses
■ children under 6 months: Ask a doctor
- Other information
-
Inactive ingredients
water, C12-15 alkyl benzoate, isopropyl palmitate, butyloctyl salicylate, ethylhexyl isononanoate, cetyl PEG/PPG-10/1 dimethicone, propylene glycol, cyclopentasiloxane, bis-octyldodecyl dimer dilinoleate/propanediol copolymer, dimethicone, ethylhexyl pelargonate, ethylhexyl methoxycrylene, polyester-27, tocopherol, PEG-12 dimethicone crosspolymer, triethoxycaprylylsilane, beeswax, hydroxyacetophenone, sodium chloride, 1,2-hexanediol, caprylyl glycol
- Questions?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
COPPERTONE PURE AND SIMPLE KIDS SUNCREEN SPF 50
zinc oxide 24.08% lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66800-2744 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 24.08 g in 100 g Inactive Ingredients Ingredient Name Strength ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) WATER (UNII: 059QF0KO0R) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) SYNTHETIC BEESWAX (UNII: 08MNR5YE2R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ETHYLHEXYL PELARGONATE (UNII: 3YU1SQ04DV) TOCOPHEROL (UNII: R0ZB2556P8) POLYESTER-7 (UNII: 0841698D2F) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM CHLORIDE (UNII: 451W47IQ8X) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) BIS-OCTYLDODECYL DIMER DILINOLEATE/PROPANEDIOL COPOLYMER (UNII: TY3J98ZR7R) ETHYLHEXYL ISONONANOATE (UNII: I6KB4GE3K4) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X) PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) Product Characteristics Color white (White to Off-White) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66800-2744-6 177 g in 1 TUBE; Type 0: Not a Combination Product 10/26/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 10/26/2023 Labeler - Beiersdorf Inc (001177906)