OTC Medication Information: W Lab BLOSSOM WHITE CUSHION 13 Blossom White

W LAB BLOSSOM WHITE CUSHION 13 BLOSSOM WHITE- titanium dioxide, octinoxate, octisalate, octocrylene and zinc oxide powder
WOW VENTURES

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

ACTIVE INGREDIENT

Active Ingredient: Titanium Dioxide 11.0%, Ethylhexyl Methoxycinnamate 7.0%, Ethylhexyl Salicylate 4.8%, Octocrylene 2.0%, Zinc Oxide 2.0%

INACTIVE INGREDIENT

Inactive Ingredients: Rosa Damascena Flower Water, Butylene Glycol, Cyclopentasiloxane, Cyclohexasiloxane, Glycerin, C12-15 Alkyl benzoate, PEG-30 Dipolyhydroxystearate, Niacinamide, Trimethylsiloxysilicate, PEG-10 Dimethicone, Sodium Chloride, Quaternium-18 Bentonite, Dimethicone, Iron Oxides (CI 77492), Ozokerite, Copernicia Cerifera (Carnauba) Wax, Triethoxycaprylylsilane, Chlorphenesin, Iron Oxides (CI 77491), Aluminum Hydroxide (CI 77002), Phenoxyethanol, Perfume, Water, Iron Oxides (CI 77499), Adenosine, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Trehalose, Melaleuca Alternifolia (Tea Tree) Leaf Water, Rubus Idaeus (Raspberry) Fruit Extract, Oenothera Biennis (Evening Primrose) Flower Extract, Vaccinium Angustifolium (Blueberry) Fruit Extract, Bambusa Vulgaris Water, Lilium Candidum Bulb Extract, Xylitylglucoside, Propanediol, Rosmarinus Officinalis (Rosemary) Leaf Water, Propylene Glycol, Melissa Officinalis Flower/Leaf/Stem Water, Anhydroxylitol, Alcohol, Xylitol, Origanum Majorana Leaf Extract, Leontopodium Alpinum Extract, 1,2-Hexanediol, Lavandula Angustifolia (Lavender) Flower, Phyllanthus Emblica Fruit Extract, Angelica Archangelica Root Extract, Centella Asiatica Extract, Salicornia Herbacea Extract, Gentiana Lutea Root Extract, Achillea Millefolium Extract, Artemisia Vulgaris Extract, Arnica Montana Flower Extract, Portulaca Oleracea Extract, Chamomilla Recutita (Matricaria) Flower Extract, Vitex Agnus Castus Extract, Plankton Extract, Camellia Japonica Flower Extract, Viola Tricolor Extract, Rubus Fruticosus (Blackberry) Fruit Extract, Potassium Sorbate, Sodium Hyaluronate, Citric Acid, Sodium Benzoate, Euterpe Oleracea Fruit Extract, Arginine Ferulate, Calendula Officinalis Flower Extract, Hydrolyzed Hyaluronic Acid

PURPOSE

Purpose: Make Up Base(Coverage), Brightening, Skin Protectant , Sunscreen

WARNINGS

Warnings: 1. Stop using the product if there is any of the following abnormal symptoms appeared after use and consult with your dermatologist as continued use can worsen the symptoms. A) if there are red spots, swelling, itchiness, or irritation B) if the above symptoms appear around the skin to which the product has been applied, after being exposed to direct sunlight. 2. Do not apply the product to any parts of the skin with wound, eczema, or dermatitis. 3. Precautions on storage and handling. A) Make sure to close the cap after use. B) Keep out of the reach of children and babies. C) Do not keep the product in a hot or cold place or a place getting direct sunlight.

DESCRIPTION

Indications & usage: Take an adequate amount and apply it to to your face by tapping with a puff gently and evenly.

Dosage & Administration: Apply it to your face by tapping with a puff gently and evenly.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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W LAB BLOSSOM WHITE CUSHION 13 BLOSSOM WHITE
titanium dioxide, octinoxate, octisalate, octocrylene, zinc oxide powder
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:69894-460
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Titanium Dioxide (TITANIUM DIOXIDE) Titanium Dioxide 1.65 g in 15 g
Octinoxate (OCTINOXATE) Octinoxate 1.05 g in 15 g
Octisalate (OCTISALATE) Octisalate 0.72 g in 15 g
Octocrylene (OCTOCRYLENE) Octocrylene 0.30 g in 15 g
Zinc Oxide (ZINC CATION) ZINC CATION 0.30 g in 15 g
Inactive Ingredients
Ingredient Name Strength
Butylene Glycol
Glycerin
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:69894-460-02 1 CONTAINER in 1 CARTON contains a CONTAINER (69894-460-01)
1 NDC:69894-460-01 15 g in 1 CONTAINER This package is contained within the CARTON (69894-460-02)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part352 10/10/2016
Labeler — WOW VENTURES (688731080)
Registrant — WOW VENTURES (688731080)
Establishment
Name Address ID/FEI Operations
WOW VENTURES 688731080 repack (69894-460)
Establishment
Name Address ID/FEI Operations
Hankook Cosmetics Manufacturing Co.,Ltd_Eumseong Factory 688235645 manufacture (69894-460)

Revised: 10/2016 WOW VENTURES

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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