SANIZER KIDS Multi-Purpose Sanitizer Spray

SANIZER KIDS Multi-Purpose Sanitizer by

Drug Labeling and Warnings

SANIZER KIDS Multi-Purpose Sanitizer by is a Otc medication manufactured, distributed, or labeled by Zermat Internacional S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SANIZER KIDS MULTI-PURPOSE SANITIZER- alcohol spray 
Zermat Internacional S.A. de C.V.

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SANIZER KIDS Multi-Purpose Sanitizer Spray

Drug Facts

Active ingredient[s]

Alcohol 80% v/v

Purpose

Antiseptic

Use[s]:

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings:

For external use only. Flammable. Keep away from heat or flame.

Do not use:

In children less than 2 months of age. On open skin wounds.

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water.

Stop use and ask a doctor

if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Directions

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

  • Store between  15-30°C (59-86°F)
  • Avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients:

Blue No.1 C.I. 42090, Fragrance, Propylene Glycol, Purified water.

Package Labeling:

Bottle

SANIZER KIDS MULTI-PURPOSE SANITIZER 
alcohol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 15828-197
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.8 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 15828-197-0163 mL in 1 BOTTLE; Type 0: Not a Combination Product11/13/202005/30/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)11/13/202005/30/2024
Labeler - Zermat Internacional S.A. de C.V. (812820712)

Revised: 6/2024
Document Id: 1a12b3b6-538a-05b9-e063-6394a90a60bf
Set id: 43c356bd-4a2f-4dc3-9615-b0a04430d57c
Version: 4
Effective Time: 20240604