EELHOE SUN CREAM- titanium dioxide cream

EELHOE Sun Cream by

Drug Labeling and Warnings

EELHOE Sun Cream by is a Otc medication manufactured, distributed, or labeled by Shantou Eelhoe Daily Chemical Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

CENTELLA ASIATICA TRITERPENOIDS

PURPOSE

Prevent ultraviolet radiation and reduce skin sunburn.

WHEN USING

1.Take an appropriate amount of this product on the fingertips.

2.Apply to areas requiring sun protection.

3.Pat gently to make it fully absorbed.

4.Wait a few minutes to play a role.

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
ISONONYL ISONONANOATE
GLYCERYL STEARATE
TITANIUM DIOXIDE
HYALURONIC ACID

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EELHOE SUN CREAM 
titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85064-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J) (CENTELLA ASIATICA TRITERPENOIDS - UNII:4YS74Q4G4J)	CENTELLA ASIATICA TRITERPENOIDS	0.004 mg  in 40 mg

Inactive Ingredients
Ingredient Name	Strength
OCTINOXATE (UNII: 4Y5P7MUD51)	2 mg  in 40 mg
HYALURONIC ACID (UNII: S270N0TRQY)	0.004 mg  in 40 mg
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)	0.4 mg  in 40 mg
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)	1.6 mg  in 40 mg
AQUA (UNII: 059QF0KO0R)	35.592 mg  in 40 mg
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)	0.4 mg  in 40 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85064-004-01	40 mg in 1 BOX; Type 0: Not a Combination Product	03/15/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/15/2025

Labeler - Shantou Eelhoe Daily Chemical Technology Co., Ltd. (617290813)

Registrant - Shantou Eelhoe Daily Chemical Technology Co., Ltd. (617290813)

Establishment
Name	Address	ID/FEI	Business Operations
Shantou Eelhoe Daily Chemical Technology Co., Ltd.		617290813	manufacture(85064-004)