Label: DUKE CANNON SUPPLY CO. DAILY DEFENSE FACE MINERAL SUNSCREEN BROAD SPECTRUM SPF 32- zinc oxide lotion
- NDC Code(s): 71782-201-03
- Packager: DUKE CANNON SUPPLY CO.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2023
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- Official Label (Printer Friendly)
- Actrive Ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children.
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Directions
• Apply liberally 15 minutes before sun exposure
• Reapply: • after 80 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 10 a.m. – 2 p.m. • wear long-sleeved shirts, pants, hats and sunglasses - Other information
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Inactrive Ingredients
aloe barbadensis leaf juice, ascorbic acid, bisabolol, butyloctyl salicylate, caffeine, caprylic/capric triglyceride, cetearyl alcohol, dimethicone, ethyl ferulate, farnesol, fragrance, gluconolactone, glycerin, glyceryl stearate, helianthus annuus (sunflower) seed oil, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, isohexadecane, olive oil polyglyceryl-6 esters, panax ginsing root extract, phenoxyethanol, polysorbate 60, polysorbate 80, sodium benzoate, sodium stearoyl lactylate, sorbitan isostearate, tetrasodium glutamate diacetate, tocopherol, triethoxycaprylylsilane, VP/hexadecene copolymer, water, xanthan gum
- Label
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INGREDIENTS AND APPEARANCE
DUKE CANNON SUPPLY CO. DAILY DEFENSE FACE MINERAL SUNSCREEN BROAD SPECTRUM SPF 32
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71782-201 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 150 mg in 1 mL Inactive Ingredients Ingredient Name Strength CAPRYLIC/CAPRIC ACID (UNII: DI775RT244) WATER (UNII: 059QF0KO0R) POLYSORBATE 60 (UNII: CAL22UVI4M) POLYSORBATE 80 (UNII: 6OZP39ZG8H) ISOHEXADECANE (UNII: 918X1OUF1E) GLUCONOLACTONE (UNII: WQ29KQ9POT) VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9) SUNFLOWER OIL (UNII: 3W1JG795YI) XANTHAN GUM (UNII: TTV12P4NEE) ETHYL FERULATE (UNII: 5B8915UELW) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) PHENOXYETHANOL (UNII: HIE492ZZ3T) OLIVE OIL POLYGLYCERYL-6 ESTERS (UNII: 4KDO9AFM9I) SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) SODIUM BENZOATE (UNII: OJ245FE5EU) GLYCERIN (UNII: PDC6A3C0OX) PEG-20 SORBITAN ISOSTEARATE (UNII: X958PZJ9ON) BISABOLOL OXIDE A (UNII: 16AE65F94Y) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) ALOE VERA LEAF (UNII: ZY81Z83H0X) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) CAFFEINE (UNII: 3G6A5W338E) ASCORBIC ACID (UNII: PQ6CK8PD0R) ASIAN GINSENG (UNII: CUQ3A77YXI) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71782-201-03 1 in 1 BOX 11/27/2023 1 88 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 11/27/2023 Labeler - DUKE CANNON SUPPLY CO. (078715221)
