Label: ABC ARBONNE BABY CARE SUNSCREEN BROAD SPECTRUM SPF 30 WATER-RESISTANT (40 MINUTES)- zinc oxide lotion
- NDC Code(s): 42508-332-02
- Packager: Arbonne International, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 12, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
-
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
- apply liberally 15 minutes before sun exposure
- reapply:
- after 40 minutes of swimming or sweating
- immediately after towel drying
- at least every 2 hours
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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
- children under 6 months of age: ask a doctor
- Other information
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Inactive ingredients
water, C12-15 alkyl benzoate, caprylic/capric triglyceride, coco-caprylate, polyglyceryl-2 dipolyhydroxystearate, dicaprylyl carbonate, polyglyceryl-4 isostearate, cetyl dimethicone, glycerin, copernicia cerifera (carnauba) wax, cetyl alcohol, euphorbia cerifera (candelilla) wax, tapioca starch, calendula officinalis flower extract, chamomilla recutita (matricaria) flower extract, aloe barbadensis leaf juice, triethoxycaprylylsilane, tocopheryl acetate, magnesium sulfate, sodium chloride, silica dimethyl silylate, stearic acid, chlorphenesin, phenoxyethanol.
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 177 mL Tube Carton
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INGREDIENTS AND APPEARANCE
ABC ARBONNE BABY CARE SUNSCREEN BROAD SPECTRUM SPF 30 WATER-RESISTANT (40 MINUTES)
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:42508-332 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 144 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) COCO-CAPRYLATE (UNII: 4828G836N6) POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7) CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB) GLYCERIN (UNII: PDC6A3C0OX) CARNAUBA WAX (UNII: R12CBM0EIZ) CETYL ALCOHOL (UNII: 936JST6JCN) CANDELILLA WAX (UNII: WL0328HX19) STARCH, TAPIOCA (UNII: 24SC3U704I) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CHAMOMILE (UNII: FGL3685T2X) ALOE VERA LEAF (UNII: ZY81Z83H0X) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) SODIUM CHLORIDE (UNII: 451W47IQ8X) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) STEARIC ACID (UNII: 4ELV7Z65AP) CHLORPHENESIN (UNII: I670DAL4SZ) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42508-332-02 1 in 1 CARTON 06/30/2023 08/16/2026 1 177 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 06/30/2023 08/16/2026 Labeler - Arbonne International, LLC (961643454)
