TOK AND CARE SANITIZER- hypochlorous acid liquid

TOK AND CARE SANITIZER by

Drug Labeling and Warnings

TOK AND CARE SANITIZER by is a Otc medication manufactured, distributed, or labeled by KEWS CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Hypochlorous Acid ------ 0.0.007%

Purpose

Antimicrobial

Directions:

Use when soap and water not available to supplement regular hand washing.

Press the front fingerprint shape to wash hands, skin.

Or rub hands with a tissue

Rub suspected tool, furniture, and space.

Inactive Ingredient(s)

Water

Intended Use

For Personal sanitizing to decrease virus and baceteria on skin

Warnings:

For external use only

Purpose:

For personal sanitizing to decrease virus and bacteria on skin

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

0.27 fl oz (8 mL) PDP

0.27 fl oz (8mL) NDC: 75644-004-01

0.27fl oz (8ml ea) X 10 Pouches PDP

0.27 fl oz (8ml) X 10 Pouches NDC: 75644-004-02

1.69 fl oz (50ml) PDP

1.69 fl oz (50ml) PDP 75644-004-03

3.38 Fl oz (100ml) PDP

3.38 Fl oz (100ml) PDP, NDC: 75644-004-04

INGREDIENTS AND APPEARANCE

TOK AND CARE SANITIZER 
hypochlorous acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75644-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10)	HYPOCHLOROUS ACID	0.007 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75644-004-03	50 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/18/2021
2	NDC: 75644-004-04	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/18/2021
3	NDC: 75644-004-02	10 in 1 BOX	06/18/2021
3	NDC: 75644-004-01	8 mL in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 75644-004-01	8 mL in 1 POUCH; Type 0: Not a Combination Product	06/18/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/18/2021

Labeler - KEWS CORPORATION (688640317)

Registrant - KEWS CORPORATION (688640317)

Establishment
Name	Address	ID/FEI	Business Operations
KEWS CORPORATION		688640317	pack(75644-004) , manufacture(75644-004) , label(75644-004)