Label: YES TO CUCUMBERS DAILY MOISTURIZER SPF 30- zinc oxide, titanium dioxide lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 51514-0321-1 - Packager: Autumn Harp, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated October 3, 2013
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- DESCRIPTION
- Active Ingredients
- Purpose
- Uses
- Warnings:
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Directions
Apply liberally 15 minutes before sun exposure. Use a water resistant sunscreen if swimming or sweating. Reapply at least every 2 hours. Children under 6 months: Ask a doctor.
Sun Protection Mesaure Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with Broad Spectrum SPF value of 15 or higher and other sun measures including: Limit time in the sun, especially from 10 am - 2 pm. Wear long-sleeved shirts, pants, hats, and sun-glasses
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Inactive Ingredients
Water, Ethylhexyl Palmitate, Hydrogenated Methyl Abietate, Glycerin, Glyceryl Stearate Citrate, Magnesium Aluminum Silicate, Aluminum Hydroxide, Cetearyl Alcohol, Phenethyl Alcohol, Sodium Magnesium Silicate, Glyceryl Caprylate, Xanthan Gum, Alcohol, Fragrance, Hydrated Silica, Triethoxycaprylylsilane, Tocopherol, Aloe Barbadensis Leaf Juice, Maris Limus Extract, Cumumis Sativus (Cucumber) Seed Extract*, Camellia Sinensis (Green Tea) Leaf Extract, Citric Acid, Potassium Sorbate, Sodium Benzoate. * Certified Organic Ingredient
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INGREDIENTS AND APPEARANCE
YES TO CUCUMBERS DAILY MOISTURIZER SPF 30
zinc oxide, titanium dioxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51514-0321 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 11.0 mg in 100 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 6.2 mg in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ETHYLHEXYL PALMITATE (UNII: 2865993309) HYDROGENATED METHYL ABIETATE (UNII: A23O709X8O) GLYCERYL STEARATE CITRATE (UNII: WH8T92A065) GLYCERIN (UNII: PDC6A3C0OX) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) PHENETHYL ALCOHOL (UNII: ML9LGA7468) LAPONITE (UNII: D703131383) XANTHAN GUM (UNII: TTV12P4NEE) GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A) HYDRATED SILICA (UNII: Y6O7T4G8P9) ALCOHOL (UNII: 3K9958V90M) CUCUMBER (UNII: YY7C30VXJT) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) TOCOPHEROL (UNII: R0ZB2556P8) ALOE VERA LEAF (UNII: ZY81Z83H0X) CUCUMBER SEED (UNII: BT3S9L53JK) SOYBEAN OIL (UNII: 241ATL177A) GREEN TEA LEAF (UNII: W2ZU1RY8B0) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) potassium hydroxide (UNII: WZH3C48M4T) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51514-0321-1 41 mL in 1 BOTTLE, PUMP Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/06/2013 Labeler - Autumn Harp, Inc. (064187883) Establishment Name Address ID/FEI Business Operations Autumn Harp, Inc. 064187883 manufacture(51514-0321)
