BULUBIU FACE SUNSCREEN SKINCARE- sunscreen skincare cream

Bulubiu Face Sunscreen SKINCARE by

Drug Labeling and Warnings

Bulubiu Face Sunscreen SKINCARE by is a Otc medication manufactured, distributed, or labeled by Shenzhen Xiaomai Manufacturing Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Homosalate 10%

Meradimate 5%

Octinoxate 5%

Octocrylene 2%

Zinc oxide 6.3%

Purpose

Sunscreen

Moisturizes throughout theday & helps protects

Uses

Apply sunscreen generously to exposedskin. Rub it in evenly. Reapply as neededespecially after swimming or sweating.Enjoy your sun-protected day!

Wamings

For exteral use only

Do not use

on damaged or broken skin

When using this product

Only for external use. do not ingest.

Avoid direct contact with eyes.

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.

Ask Doctor

When Pregnant or breast-feeding.

Directions

Apply sunscreen generously to exposedskin. Rub it in evenly. Reapply as neededespecially after swimming or sweatingEnjoy your sun-protected day!

Other information

Before use, read all information on thecarton Store at controlled room temperature20 to 25 C (68 to 77°F)

Inactive ingredients

water, niacinamide, cetearyl alcohol, glycerin, dimethicone, behentrimonium methosulfate. ceramide 3，ceramide 6-Il. ceramide 1， hyaluronic acid， sodium hydroxide.，aluminum starch octenvlsuccinate，hydroxyethylcellulose, methylparaben, disodium EDTA, propylparaben.propylparaben, sodium lauroyl lactylate, phytosphingosine, cholesterol, carbomer, xanthan gum

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BULUBIU FACE SUNSCREEN SKINCARE 
sunscreen skincare cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83872-014
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	5 mg  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83872-014-01	50 g in 1 BOTTLE; Type 0: Not a Combination Product	01/16/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/16/2024

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

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Xiaomai Manufacturing Co., Ltd.		712999147	manufacture(83872-014)