ACTIVE INGREDIENT

Niacinamide: 2%
Sodium Hyaluronate: 0.5%
Hyaluronic Acid: 0.1%
Tocopherol: 0.2%
Ethylhexyl Methoxycinnamate: 5%
Octocrylene: 4%
Zinc Oxide: 3%
Centella Asiatica Extract: 1%
Camellia Sinensis Leaf Extract: 1%

PURPOSE

helps prevent sunburn.

Uses

decreases the risk of skin cancer and early skin aging caused by the sun.

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 swallowed, get medical
help or contact a Poison Control Center right away.

Directions

apply liberally 15 minutes before sun exposure.
reapply at least every 2 hours.
use a water resistant sunscreen if swimming or sweating.

INACTIVE INGREDIENT

Aqua: 65%
Glycerin: 3%
Cetearyl Alcohol: 2%
Butylene Glycol: 3%
Ethylhexylglycerin: 0.1%
Xanthan Gum: 0.2%
Phenoxyethanol: 0.8%
Carbomer: 0.2%
Coco-Caprylate/Caprate: 5%
Triethoxycaprylylsilane: 0.1%
Dibutyl Adipate: 2%
Polymethylsilsesquioxane: 1.7%
Linalool: 0.1%

Other Information

Protect the product in this container from excessive heat and
direct sun.

BULUBIU UNSEEN SUNSCREEN SPF 50
unseen sunscreen cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:83872-033
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	20 mg in 1 g
TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8)	TOCOPHEROL	2 mg in 1 g
HYALURONIC ACID (UNII: S270N0TRQY) (HYALURONIC ACID - UNII:S270N0TRQY)	HYALURONIC ACID	1 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
GLYCERIN (UNII: PDC6A3C0OX)	30 mg in 1 g
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)	30 mg in 1 g
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)	1 mg in 1 g

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:83872-033-01	50 g in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2024

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M016	03/15/2024

Labeler - Shenzhen XiaoMai Manufacturing Co., Ltd. (712999147)

Name	Address	ID/FEI	Business Operations
Establishment
Shenzhen XiaoMai Manufacturing Co., Ltd.		712999147	manufacture(83872-033)