Label: NEUTROGENA MINERAL BEACH DEFENSE ON-THE-GO BODY SPF 50- zinc oxide stick
- NDC Code(s): 69968-0775-2
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 13, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Purpose
- Uses
- Warnings
-
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
- 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
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 42 g Canister
-
INGREDIENTS AND APPEARANCE
NEUTROGENA MINERAL BEACH DEFENSE ON-THE-GO BODY SPF 50
zinc oxide stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0775 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 216 mg in 1 g Inactive Ingredients Ingredient Name Strength ADIPIC ACID/DIGLYCOL CROSSPOLYMER (20000 MPA.S) (UNII: R9TPS68K19) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) NEOPENTYL GLYCOL DIISOSTEARATE (UNII: 4M6OQ34JWW) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) PARAFFIN (UNII: I9O0E3H2ZE) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C) CERESIN (UNII: Q1LS2UJO3A) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0775-2 42 g in 1 CANISTER; Type 0: Not a Combination Product 10/31/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 10/31/2022 Labeler - Kenvue Brands LLC (118772437)
