Label: YOUTH CORRIDOR SOOTHE AND DEFEND SPF-30- octocrylene, octisalate, zinc oxide cream
- NDC Code(s): 81201-111-00
- Packager: Youth Corridor
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses:
- Warnings:
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Directions:
- Apply liberally 15 minutes before sun exposure.
- Children under 6 months of age:ask a doctor
- Reapply at least every 2 hours.
- Reapply as needed or after towel drying, swimming, or sweating
- Use a water-resistant sunscreen if swimming or sweating.
- 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: Sun Protection Measures:
- limit time in the sun, especially from 10a.m. - 2.p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses.
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Inactive Ingredients:
Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), C12-15 Alkyl Benzoate, C13-14 Isoparaffin, Camellia Sinesis (Green Tea)Extract, Cetyl Alcohol, Cucumis Sativus (Cuumber) Extract, Dimethicone, Dodecane, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Glycyrrhiza Glabra (Licorice) Extract, Helianthus Annuss(Sunflower)Oil, Laureth-7, PEG-100 Stearate, Phenoxyethanol, Polyacrylamide, Polysorbate-20, Prunus Amygdalus, Dulcis (Almond)Oil, Stearic Acid, Tocopherol Acetate (Vitamin E), Triethanolamine, Zemea (Corn) Propanediol.
- Other information:
- Questions?
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
YOUTH CORRIDOR SOOTHE AND DEFEND SPF-30
octocrylene, octisalate, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81201-111 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 80 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CETYL ALCOHOL (UNII: 936JST6JCN) CUCUMBER (UNII: YY7C30VXJT) DIMETHICONE (UNII: 92RU3N3Y1O) DODECANE (UNII: 11A386X1QH) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) LICORICE (UNII: 61ZBX54883) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) LAURETH-7 (UNII: Z95S6G8201) PEG-100 STEARATE (UNII: YD01N1999R) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 20 (UNII: 7T1F30V5YH) ALMOND (UNII: 3Z252A2K9G) STEARIC ACID (UNII: 4ELV7Z65AP) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TROLAMINE (UNII: 9O3K93S3TK) CORN (UNII: 0N8672707O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81201-111-00 60 mL in 1 CYLINDER; Type 0: Not a Combination Product 12/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/01/2020 Labeler - Youth Corridor (021181182)
