OUHOE ALOE SOOTHING SUN CREAM- glycerin cream

OUHOE Aloe Soothing Sun Cream by

Drug Labeling and Warnings

OUHOE Aloe Soothing Sun Cream 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

ALOE VERA LEAF

PURPOSE

Formulated with Aloe Leaf Extract , this sun cream protects skin against UVA & UVB rays keep the skin moist and smooth, and provide sufficient sunscreen effect.

WHEN USING

15-20 minutes before going out, apply the sunscreen evenly on the face or body where the sunscreen is required, massage until fully absorbed, and then form a film .If you need to apply makeup, please use it before makeup. If exposed to the sun for a long time, it needs to be reapplied every 2-3 hours.

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.

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.

STORAGE AND HANDLING

Store in a cool and dry place.

INACTIVE INGREDIENT

AQUA
ETHYLHEXYL METHOXYCINNAMATE
OCTOCRYLENE
ISONONYL ISONONANOATE
GLYCERIN

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

OUHOE ALOE SOOTHING SUN CREAM 
glycerin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85163-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X) (ALOE BARBADENSIS LEAF - UNII:ZY81Z83H0X)	ALOE BARBADENSIS LEAF	0.05 mg  in 50 mg

Inactive Ingredients
Ingredient Name	Strength
ETHYLHEXYL METHOXYCINNAMATE (UNII: 4Y5P7MUD51)	2.5 mg  in 50 mg
OCTOCRYLENE (UNII: 5A68WGF6WM)	2.5 mg  in 50 mg
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)	2 mg  in 50 mg
GLYCERIN (UNII: PDC6A3C0OX)	0.75 mg  in 50 mg
AQUA (UNII: 059QF0KO0R)	42.2 mg  in 50 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85163-003-01	50 mg in 1 BOX; Type 0: Not a Combination Product	04/10/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	04/10/2025

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

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

Establishment
Name	Address	ID/FEI	Business Operations
Shantou Ouhoe Technology Co., Ltd.		617531875	manufacture(85163-003)