OUHOE FACE BODY SUNSCREEN- titanium dioxide cream

OUHOE Face Body Sunscreen by

Drug Labeling and Warnings

OUHOE Face Body Sunscreen by is a Otc medication manufactured, distributed, or labeled by Shantou Ouhoe Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

BEESWAX、PROPOLIS EXTRACT、OLEA EUROPAEA (OLIVE) FRUIT OIL、SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL、BUTYROSPERMUM PARKII (SHEA) BUTTER

PURPOSE

1. lt can provide long-lasting moistunzing to the skin and keep your skin soft.
2. Long-lasting sunscreen effect,protects skin from ultraviolet damage and keeps skin moist.
3. It has a light texture and can be quickly absorbed by the skin.It is not greasy or sticky and feels refreshing and comfortable after use.

WHEN USING

1. Clean and dry skin
2. Take an appropriate amount of this product and apply
it evenly on the skin
3. Wait for the sunscreen film to form before going out

WARNINGS

Please keep out of reach of children. Do not swallow.Please clean your hands before use to ensure the best results from the product. Discontinue use if signs of irritation or rash occur. Store in a cool and dry place.

DO NOT USE

Discontinue use if signs of irritation or rash occur.

STOP USE

Discontinue use if signs of irritation or rash occur.

KEEP OUT OF REACH OF CHILDREN

Please keep out of reach of children. Do not swallow.

STORAGE AND HANDLING

Store in a cool and dry place.

INACTIVE INGREDIENT

AQUA、ETHYLHEXYL METHOXYCINNAMATE、OCTOCRYLENE、ISONONYL ISONONANOATE、GLYCERYL STEARATE、TITANIUM DIOXIDE、TALLOW、ZINC OXIDE

INDICATIONS & USAGE

1. Clean and dry skin
2. Take an appropriate amount of this product and apply
it evenly on the skin
3. Wait for the sunscreen film to form before going out

DOSAGE & ADMINISTRATION

1. Clean and dry skin
2. Take an appropriate amount of this product and apply
it evenly on the skin
3. Wait for the sunscreen film to form before going out

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

OUHOE FACE BODY SUNSCREEN 
titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85163-017
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL (UNII: 724GKU717M) (SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL - UNII:724GKU717M)	SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL	0.016 mg  in 80 mg
PROPOLIS WAX (UNII: 6Y8XYV2NOF) (PROPOLIS WAX - UNII:6Y8XYV2NOF)	PROPOLIS WAX	0.016 mg  in 80 mg
OLEA EUROPAEA (OLIVE) FRUIT OIL (UNII: 6UYK2W1W1E) (OLEA EUROPAEA (OLIVE) FRUIT OIL - UNII:6UYK2W1W1E)	OLEA EUROPAEA (OLIVE) FRUIT OIL	0.016 mg  in 80 mg
BEESWAX (UNII: 2ZA36H0S2V) (BEESWAX - UNII:2ZA36H0S2V)	BEESWAX	0.016 mg  in 80 mg
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y) (BUTYROSPERMUM PARKII (SHEA) BUTTER - UNII:K49155WL9Y)	BUTYROSPERMUM PARKII (SHEA) BUTTER	0.016 mg  in 80 mg

Inactive Ingredients
Ingredient Name	Strength
GLYCERYL STEARATE (UNII: 230OU9XXE4)	1.2 mg  in 80 mg
ZINC OXIDE (UNII: SOI2LOH54Z)	0.016 mg  in 80 mg
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)	3.2 mg  in 80 mg
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)	0.8 mg  in 80 mg
AQUA (UNII: 059QF0KO0R)	65.088 mg  in 80 mg
ETHYLHEXYL METHOXYCINNAMATE (UNII: 4Y5P7MUD51)	4.8 mg  in 80 mg
OCTOCRYLENE (UNII: 5A68WGF6WM)	4.8 mg  in 80 mg
TALLOW (UNII: 98HPY76U4W)	0.016 mg  in 80 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85163-017-01	80 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/26/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/26/2025

Labeler - Shantou Ouhoe Technology Co., Ltd. (617531875)

Establishment
Name	Address	ID/FEI	Business Operations
Shantou Ouhoe Technology Co., Ltd.		617531875	manufacture(85163-017)