Label: BADABOOM SUNSCREEN- sunscreen cream
- NDC Code(s): 82723-002-01
- Packager: Aopline Health Industry Technology (Guangzhou) Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated March 8, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
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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 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-sleeve shirts, pants, hats, and sunglasses.
children under 6 months: ask a doctor. - Other Information
- Inactive Ingredients
- Keep out of reach of children.
- Stop use
- WHEN USING
- Do not use
- Package Label
-
INGREDIENTS AND APPEARANCE
BADABOOM SUNSCREEN
sunscreen creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82723-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 23.9 g in 100 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 24.1 g in 100 g Inactive Ingredients Ingredient Name Strength CERAMIDE NP (UNII: 4370DF050B) HYALURONATE SODIUM (UNII: YSE9PPT4TH) ETHYL ACRYLATE AND METHYL METHACRYLATE COPOLYMER DISPERSION (2:1; 600000 MW 30% AQUEOUS) (UNII: 3EW60Z566Z) .ALPHA.-TOCOPHEROL CALCIUM SUCCINATE, DL- (UNII: H5A1374A6R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82723-002-01 4.5 g in 1 BOX; Type 0: Not a Combination Product 05/07/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 05/07/2022 Labeler - Aopline Health Industry Technology (Guangzhou) Co., Ltd. (715076108) Establishment Name Address ID/FEI Business Operations Aopline Health Industry Technology (Guangzhou) Co., Ltd. 715076108 manufacture(82723-002)
