BADABOOM SUNSCREEN- sunscreen cream

BADABOOM SUNSCREEN by

Drug Labeling and Warnings

BADABOOM SUNSCREEN by is a Otc medication manufactured, distributed, or labeled by Aopline Biotechnology (Guangzhou) Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc Oxide 24.1%
Titanium Dioxide 23.9%

PURPOSE

Sunscreen

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If product is swallowed , get medical help or contact a Poison Control Center right away.

WARNINGS

For external use only.
Do not use on damaged or broken skin.
When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if rash occurs.
Keep out of reach of children. If product is swallowed , get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

apply liberally 15 minutes before sun exposure.
reapply :after 80 minutes of swimming or sweating.
immediately after towel drying.
at least every 2 hours.

INDICATIONS & USAGE

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.

INACTIVE INGREDIENT

Ascorbic Acid ( Vitamin C ) , Camellia Sinensis Leaf Extract , Ceramide EOP, CI 77491 , CI 77492 , Mica , Polymethyl Methacrylate , Silica , Sodium Hyaluronate( Hyaluronic Acid ) , Tocopherol ( Vitamin E )

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BADABOOM SUNSCREEN 
sunscreen cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87283-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	24.1 g  in 100 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	23.9 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
CI 77492 (UNII: EX438O2MRT)
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
CERAMIDE 9 (UNII: 88KCS7120E)
CI 77491 (UNII: 1K09F3G675)
CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
MICA (UNII: V8A1AW0880)
SILICA (UNII: ETJ7Z6XBU4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87283-002-01	4.5 g in 1 BOX; Type 0: Not a Combination Product	01/08/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/08/2026

Labeler - Aopline Biotechnology (Guangzhou) Co., Ltd. (514879104)

Registrant - Aopline Biotechnology (Guangzhou) Co., Ltd. (514879104)