ODLUMIVIE TINTED MINERAL SUNSCREEN- zinc oxide,titanium dioxide cream

ODLUMIVIE Tinted Mineral Sunscreen by

Drug Labeling and Warnings

ODLUMIVIE Tinted Mineral Sunscreen by is a Otc medication manufactured, distributed, or labeled by Guangzhou Meijiao Medical Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc Oxide ..... 6.0% ..... Sunscreen
Titanium Dioxide ..... 4.5% ..... Sunscreen

INACTIVE INGREDIENT

INACTIVE INGREDIENTS:
Water
Ethylhexyl Palmitate
Cetyl Ethylhexanoate
Tinosorb S (Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine)
Butyloctyl Salicylate
Pentaerythrityl Tetraethylhexanoate
Potassium Cetyl Phosphate
Cetearyl Alcohol
Hemisqualane
Silica
Glyceryl Stearate
Sodium PCA
Panthenol
Niacinamide
Ascorbyl Glucoside
Sodium Hyaluronate
Acetylated Sodium Hyaluronate
Cross-linked Sodium Hyaluronate
Hydrolyzed Sodium Hyaluronate
Polypodium Leucotomos Extract
Green Tea Extract
Fullerene
Collagen Peptide
Pro-Xylane
Tri(Cetearyl-4) Phosphate
Aluminum Hydroxide
Stearic Acid
Tocopheryl Acetate
Natural Bisabolol

PURPOSE

Helps prevent sunburn. If used as directed with other sun protection measures (see Directions), it helps minimize signs of UV-induced skin aging.

WARNINGS

WARNINGS:
For external use only. Avoid contact with eyes. Discontinue use if irritation occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DO NOT USE

DO NOT USE:
Do not use on damaged or broken skin.
Do not use if you are allergic to any of the ingredients in this product.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center right away.

STOP USE

STOP USE AND ASK A DOCTOR IF:
Irritation or rash develops.

INDICATIONS & USAGE

DIRECTIONS:
Apply to clean, dry skin 15 minutes before sun exposure. Reapply every 2 hours or after swimming, sweating, or towel drying.

WHEN USING

WHEN USING THIS PRODUCT:
Keep out of eyes. Rinse with water to remove.

DOSAGE & ADMINISTRATION

Apply to clean, dry skin 15 minutes before sun exposure. Reapply every 2 hours or after swimming, sweating, or towel drying. use 1-2ml on targeting areas

PRINCIPAL DISPLAY PANEL

DRUG FACTS

Active Ingredients Purpose
Zinc Oxide 6.0% Sunscreen
Titanium Dioxide 4.5% Sunscreen

USES:
Helps prevent sunburn. If used as directed with other sun protection measures (see Directions), it helps minimize signs of UV-induced skin aging.

WARNINGS:
For external use only. Avoid contact with eyes. Discontinue use if irritation occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS:
Apply to clean, dry skin 15 minutes before sun exposure. Reapply every 2 hours or after swimming, sweating, or towel drying.

OTHER INFORMATION:
Store at 15–40°C (59–104°F). Keep container tightly closed and avoid extreme heat or direct sun exposure.

INACTIVE INGREDIENTS:
Water, Ethylhexyl Palmitate, Cetyl Ethylhexanoate, Tinosorb S (Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine), Butyloctyl Salicylate, Pentaerythrityl Tetraethylhexanoate, Potassium Cetyl Phosphate, Cetearyl Alcohol, Hemisqualane, Silica, Glyceryl Stearate, Sodium PCA, Panthenol, Niacinamide, Ascorbyl Glucoside, Sodium Hyaluronate, Acetylated Sodium Hyaluronate, Cross-linked Sodium Hyaluronate, Hydrolyzed Sodium Hyaluronate, Polypodium Leucotomos Extract, Green Tea Extract, Fullerene, Collagen Peptide, Pro-Xylane, Tri(Cetearyl-4) Phosphate, Aluminum Hydroxide, Stearic Acid, Tocopheryl Acetate, Natural Bisabolol

INGREDIENTS AND APPEARANCE

ODLUMIVIE TINTED MINERAL SUNSCREEN 
zinc oxide,titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87036-036
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	4.5 g  in 100 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	6 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
STEARIC ACID (UNII: 4ELV7Z65AP)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
FULLERENES (UNII: NP9U26B839)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
WATER (UNII: 059QF0KO0R)
NIACINAMIDE (UNII: 25X51I8RD4)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
PANTHENOL (UNII: WV9CM0O67Z)
HYDROXYPROPYL TETRAHYDROPYRANTRIOL (UNII: 4U3GMG1OT1)
BISABOLOL (UNII: 24WE03BX2T)
TRICETEARETH-4 PHOSPHATE (UNII: 69534Y66NO)
SILICA (UNII: ETJ7Z6XBU4)
SODIUM PCA (UNII: 469OTG57A2)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
PENTAERYTHRITYL TETRAETHYLHEXANOATE (UNII: XJ7052W897)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE (UNII: PWZ1720CBH)
CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
ASCORBYL TOCOPHERYL MALEATE (UNII: D2G6259XR5)

Product Characteristics
Color	brown	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87036-036-01	60 g in 1 TUBE; Type 0: Not a Combination Product	01/08/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/08/2026

Labeler - Guangzhou Meijiao Medical Biotechnology Co., Ltd. (978211825)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Meijiao Medical Biotechnology Co., Ltd.		978211825	manufacture(87036-036)