YAN PLUS SUPER MEDIC- colloidal silver spray 
TRIPEOPLE COSMETIC CO.,LTD.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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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

Image of bottle

YAN PLUS SUPER MEDIC 
colloidal silver spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76642-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER0.004 g  in 200 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Potassium chloride (UNII: 660YQ98I10)  
SODIUM SILICATE (UNII: IJF18F77L3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76642-010-01200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/01/2020
Labeler - TRIPEOPLE COSMETIC CO.,LTD. (695004869)
Registrant - TRIPEOPLE COSMETIC CO.,LTD. (695004869)
Establishment
NameAddressID/FEIBusiness Operations
TRIPEOPLE COSMETIC CO.,LTD.695004869manufacture(76642-010)

Revised: 5/2020
Document Id: 0aebc275-f218-411d-bf65-d7be6ec6f083
Set id: cad6dbc1-9f96-44b2-9b3e-624e9e9605b0
Version: 2
Effective Time: 20200509
 
TRIPEOPLE COSMETIC CO.,LTD.