NARO TIAMO- potassium carbonate liquid

NARO TIAMO by

Drug Labeling and Warnings

NARO TIAMO by is a Otc medication manufactured, distributed, or labeled by NARO Global Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

potassium carbonate

INACTIVE INGREDIENT

ε-Polylysine.Dextrin.1,2-Propanediol.Citric Acid.Tea Catechin. Hydroxypropylmethyl Cellulose.Distilled water.

PURPOSE

Sanitizer to help decrease bacteria on skin

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

Spray on skin as needed

WARNINGS

For external use only.

When using this product

Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear.

Keep out of reach of children.

Store at room temperature.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NARO TIAMO 
potassium carbonate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81936-0003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D)	POTASSIUM CARBONATE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81936-0003-1	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/30/2021

Labeler - NARO Global Inc. (695123340)

Registrant - NARO Global Inc. (695123340)

Establishment
Name	Address	ID/FEI	Business Operations
NARO Global Inc.		695123340	manufacture(81936-0003)