Label: BADGER SPF 50 ADVENTURE SPORT MINERAL SUNSCREEN CREAM- zinc oxide cream
- NDC Code(s): 62206-5031-3
- Packager: W.S. Badger Company, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 15, 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
- DO NOT USE
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
-
Directions
- For full protection, apply liberally (2mg/cm 2 of skin) to all exposed skin 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 10am-2pm
- Wear long-sleeved shirts, pants, hats, and sunglasses
- For children under 6 months of age: ask a doctor.
- Other Information
- Inactive Ingredients
-
PRINCIPAL DISPLAY PANEL
BADGER ® ADVENTURE
Mineral Sunscreen Cream
BROAD SPECTRUM
SPF 50
WATER RESISTANT (80 MIN)
Reef Friendly
Certified to Protect Land & Sea
98% ORGANIC INGREDIENTS
WITH CLEAR ZINC
CLEAN
MOISTURIZING
CRUELTY FREE
UNSCENTED & HYPOALLERGENIC
Solar Powered
Water Free
50% Recycled Package
Protect Land + Sea Certified
NSF
Certified B Corporation
Cruelty Free
87ml / 2.9 fl oz
-
INGREDIENTS AND APPEARANCE
BADGER SPF 50 ADVENTURE SPORT MINERAL SUNSCREEN CREAM
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62206-5031 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 25 g in 100 mL Inactive Ingredients Ingredient Name Strength YELLOW WAX (UNII: 2ZA36H0S2V) TOCOPHEROL (UNII: R0ZB2556P8) SUNFLOWER OIL (UNII: 3W1JG795YI) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62206-5031-3 87 mL in 1 TUBE; Type 0: Not a Combination Product 02/15/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/15/2024 Labeler - W.S. Badger Company, Inc. (963242326) Establishment Name Address ID/FEI Business Operations W.S. BADGER COMPANY, INC. 963242326 manufacture(62206-5031)