YAN PLUS SUPER MEDIC- colloidal silver spray

Yan Plus Super Medic by

Drug Labeling and Warnings

Yan Plus Super Medic by is a Otc medication manufactured, distributed, or labeled by TRIPEOPLE COSMETIC CO.,LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients
COLLOIDAL SILVER 0.002%

INACTIVE INGREDIENT

Inactive ingredients
Water(Alkaline), Potassium chloride, Sodium Silicate

PURPOSE

Purpose: SANITIZER

WARNINGS

Warnings

For external use only. Do not spray in or near eyes.
Stop use and ask doctor if as adverse reaction occurs or persists.
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Do not use
in children less than 2 months of age: ask a doctor.
on open skin wounds
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Indications
.Surface of the skin and general objects for disinfection.
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When using this product
Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control immediately.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control immediately.

Uses

Uses
Yan Plus Super Medic Sanitizer kills 99.9% of germ on contact and are more powerful than alcohol based sanitizers.
YAN Pus Super Medic is thoroughly Lab tested to ensure the safety

Directions

Directions
Spray this evenly on the surface of the skin or the object, or rub it on the surface 2times. Will dry out soon.

Other information

Other information
No animals were used to test this product.
Recommend for repeated use.

QUESTIONS

Questions
www.tripeople.co.kr
TEL: 82-70-4350-1760

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

YAN PLUS SUPER MEDIC 
colloidal silver spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76642-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	0.004 g  in 200 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Potassium chloride (UNII: 660YQ98I10)
SODIUM SILICATE (UNII: IJF18F77L3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76642-010-01	200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/01/2020

Labeler - TRIPEOPLE COSMETIC CO.,LTD. (695004869)

Registrant - TRIPEOPLE COSMETIC CO.,LTD. (695004869)

Establishment
Name	Address	ID/FEI	Business Operations
TRIPEOPLE COSMETIC CO.,LTD.		695004869	manufacture(76642-010)