Label: ENHANCED FACIAL MOISTURIZER- octinoxate, zinc oxide lotion
- NDC Code(s): 62673-163-01
- Packager: Neoteric Cosmetics, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 7, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredients
- Purpose
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Uses
• Helps prevent sunburn
• If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.
- Warnings
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Directions
• After cleansing, apply product to face and neck
• 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 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 am-2 pm
• Wear long sleeved shirts, pants, hats and sunglasses.
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Inactive Ingredients
Water, Peroxidized Corn Oil, Soybean Oil, Dicaprylyl Carbonate, Polyacrylamide, C13-14 Isoparaffin, Laureth7, Steareth 21, Glycerin, Dimethicone, Myristyl Myristate, Petrolatum, Tocopheryl Acetate (Vitamin E), Panthanol (Vitamin B5), Green Tea Extract, Lactic Acid, Cetyl Alcohol, Xanthan Gum, Disodium EDTA, Steareth 2, Mica, Titanium Dioxide, BHT, Triethanolamine, Propylparaben, Methylparaben, Diazolidinyl Urea, Triethoxycaprylylsilane, Propylene Glycol
- Other Information
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ENHANCED FACIAL MOISTURIZER
octinoxate, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62673-163 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 0.08 mg in 1 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.05 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CORN OIL (UNII: 8470G57WFM) SOYBEAN OIL (UNII: 241ATL177A) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) LAURETH-7 (UNII: Z95S6G8201) STEARETH-21 (UNII: 53J3F32P58) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) MYRISTYL MYRISTATE (UNII: 4042ZC00DY) PETROLATUM (UNII: 4T6H12BN9U) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PANTOTHENIC ACID (UNII: 19F5HK2737) STEARETH-2 (UNII: V56DFE46J5) MICA (UNII: V8A1AW0880) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) TROLAMINE (UNII: 9O3K93S3TK) PROPYLPARABEN (UNII: Z8IX2SC1OH) METHYLPARABEN (UNII: A2I8C7HI9T) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62673-163-01 1 in 1 CARTON 01/01/2005 12/31/2024 1 28 g 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 01/01/2005 12/31/2024 Labeler - Neoteric Cosmetics, Inc. (790615181)
