Vaporal Hand Sanitizer aloe vera

Vaporal Hand Sanitizer aloe vera by

Drug Labeling and Warnings

Vaporal Hand Sanitizer aloe vera by is a Otc medication manufactured, distributed, or labeled by Operfel S.A.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

VAPORAL HAND SANITIZER ALOE VERA- alcohol gel 
Operfel S.A.

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Vaporal Hand Sanitizer aloe vera

Drug Facts

Active Ingredient(s)

Alcohol 70% 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 able.

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 eye 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.

Directions

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

Other Information

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

Inactive Ingredients

glycerin, hydrogen peroxide, water, carbomer, triethanolamine, Aloe Vera, fragrance.

Package Labeling:60ml

Package Labeling:250ml

VAPORAL HAND SANITIZER ALOE VERA 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79980-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79980-003-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/06/2020	08/07/2020
2	NDC: 79980-003-02	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/06/2020	08/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/06/2020	08/07/2020

Labeler - Operfel S.A. (935284554)

Revised: 1/2024

Document Id: 0e11caf0-1b72-31a4-e063-6394a90a54f7

34390-5

Set id: ac899186-43f5-32c5-e053-2995a90a4f8c

Version: 2

Effective Time: 20240103

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