VITABRID C12 FACE BRIGHTENING- zinc oxide powder

Vitabrid C12 Face Brightening by

Drug Labeling and Warnings

Vitabrid C12 Face Brightening by is a Otc medication manufactured, distributed, or labeled by Hyundai Bioscience Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients:
Allantoin 0.25%, Zinc Oxide 25%

INACTIVE INGREDIENT

Inactive Ingredients: Ascorbic Acid, Glyceryl Stearate, Acetyl Glucosamine, Niacinamide, Serine, Betaine, Hydrolyzed Collagen, Adenosine, Water

PURPOSE

PURPOSE: Skin Protectant

WARNINGS

Warning:
For external use only
Avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.
Do not apply to deep cuts, puncture wounds, animal bites, or serious burns.
Keep out of reach of children.
If swallowed, seek medical assistance or contact a Poison Control Center immediately.
Discontinue use and consult a physician if rash or irritation occurs.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Use

Use: Active vitamin C is released into the skin for over 12 hours to help the skin look firmer, healthier, brighter and revitalized while diminishing the appearance of fine lines and wrinkles.

Directions

Directions:
1. Shake before using to loosen the powder.
2. Mix an appropriate amount of the powder with daily skin care product of your choice (serum or moisturizer) in the palm of your hand.
3. Smooth the mixture onto clean face and neck. For best results, apply twice a day (morning and evening).
* Adjust the amount of powder depending on your skin condition.
* If you experience feelings of dryness, apply serum or moisturizer.

Other Information

Other Information:
Store between 20-25 °C (68-77 °F)
Avoid freezing and excessive heat above 40 °C (104 °F)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VITABRID C12 FACE BRIGHTENING 
zinc oxide powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70933-301
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	25 g  in 100 g
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.25 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ASCORBIC ACID (UNII: PQ6CK8PD0R)	25 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70933-301-01	3 g in 1 BOTTLE; Type 0: Not a Combination Product	07/09/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	07/09/2017

Labeler - Hyundai Bioscience Co., Ltd. (688277268)

Registrant - Hyundai Bioscience Co., Ltd. (688277268)

Establishment
Name	Address	ID/FEI	Business Operations
Hyundai Bioscience Co., Ltd.		688277268	manufacture(70933-301)