White Cloud Hand Sanitizer

White Cloud Hand Sanitizer by

Drug Labeling and Warnings

White Cloud Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Moderplas, S. de R.L. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WHITE CLOUD HAND SANITIZER- alcohol gel 
Moderplas, S. de R.L. de C.V.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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White Cloud Hand Sanitizer

Drug Facts

Active Ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Use

  • Hand sanitizer to decrease bacteria on the skin

Warnings

For external use only

Flammable, Keep away fire or flame.

When using this product

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

Stop use and ask a doctor

If irritation or rash develop and persists.

Keep out of reach of children.

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

Directions

  • Put product on your hands and rub together and between fingers until dry.
  • Children undre 6 years old, use under adult supervision.

Other information

  • Do not store above 105°F, may discolor certain fabrics or surfaces.

Inactive ingredients

Water, carbomers, glycerin, aloe vera, hydrogen peroxide.

Package Labeling:

Bottle

WHITE CLOUD HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 80477-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 80477-001-00300 mL in 1 BOTTLE; Type 0: Not a Combination Product09/04/202012/31/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E09/04/202012/31/2021
Labeler - Moderplas, S. de R.L. de C.V. (951581874)

Revised: 3/2022
Document Id: da5646b6-b597-f6f1-e053-2a95a90ad309
Set id: aefc0ce6-2b1a-205d-e053-2a95a90a6c1c
Version: 3
Effective Time: 20220316