TOK AND CARE SANITIZER- hypochlorous acid liquid 
KEWS CORPORATION

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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TOK AND CARE SANITIZER

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.

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

TOK AND CARE (8ml)

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

TOK AND CARE 8 ML 10 POUCHES0.27 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 TOK AND CARE 50ml

3.38 Fl oz (100ml) PDP

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

TOK AND CARE 100ml

TOK AND CARE SANITIZER 
hypochlorous acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75644-004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.007 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75644-004-0350 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/18/2021
2NDC:75644-004-04100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/18/2021
3NDC:75644-004-0210 in 1 BOX06/18/2021
3NDC:75644-004-018 mL in 1 POUCH; Type 0: Not a Combination Product
4NDC:75644-004-018 mL in 1 POUCH; Type 0: Not a Combination Product06/18/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/18/2021
Labeler - KEWS CORPORATION (688640317)
Registrant - KEWS CORPORATION (688640317)
Establishment
NameAddressID/FEIBusiness Operations
KEWS CORPORATION688640317pack(75644-004) , manufacture(75644-004) , label(75644-004)

Revised: 6/2021
Document Id: c4d4f02d-2d6f-67c0-e053-2a95a90a6e64
Set id: c4d4f02d-2d6e-67c0-e053-2a95a90a6e64
Version: 1
Effective Time: 20210615
 
KEWS CORPORATION