VITABRID C12 DOCTOR SENSITIVE FACE POWDER- zinc oxide powder
HYUNDAI IBT CO., LTD.

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.

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ACTIVE INGREDIENT

zinc oxide 25%

INACTIVE INGREDIENT

ascorbic acid, glyceryl stearate, acetyl glucosamine, niacinamide, etc

PURPOSE

skin protectant

WARNINGS

Warnings: 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. Stop use and ask a doctor if condition worsens or does not improve after regular use.

KEEP OUT OF REACH OF CHILDREN

Use

Active vitamin C is released into the skin for over 12 hours, and in conjunction with peptides and plant stem cells help the skin look firmer, healthier, brighter and revitalized while diminishing the appearance of fine lines and wrinkles.

Directions

apply proper amount to the skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottle

VITABRID C12 DOCTOR SENSITIVE FACE POWDER
zinc oxide powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70933-300
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	25 g in 100 g
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.3 g in 100 g

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:70933-300-01	3.5 g in 1 BOTTLE; Type 0: Not a Combination Product	06/24/2017	07/30/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part347	06/24/2017	07/30/2017

Labeler - HYUNDAI IBT CO., LTD. (688277268)

Registrant - HYUNDAI IBT CO., LTD. (688277268)

Name	Address	ID/FEI	Business Operations
Establishment
HYUNDAI IBT CO., LTD.		688277268	manufacture(70933-300)

Revised: 3/2018

Document Id: 1fc17845-e8eb-4d9e-8bfe-8ce7b4f97460

Set id: 52aad275-ca70-2137-e054-00144ff88e88

Version: 2

Effective Time: 20180316

HYUNDAI IBT CO., LTD.