ALOE VERA LEAF HAND SANITIZER

ALOE VERA LEAF HAND SANITIZER by

Drug Labeling and Warnings

ALOE VERA LEAF HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by UI Global Brands LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ALOE VERA LEAF HAND SANITIZER- alcohol gel 
UI Global Brands LLC

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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ALOE VERA LEAF HAND SANITIZER

Drug Facts

Active ingredient

Alcohol Denat. 75%

Purpose

Antimicrobial

Uses

To decrease bacteria on the skin and clean hands.  Recommended for repeated use.

Warnings

For external use only.

Flammable, keep away from fire or flame.

Keep out of reach of children. Do not get into eyes.

If contact occurs, rinse thoroughly with water.

Discontinue use

if irritation occurs or redness develops.  If irritation persists for more than 72 hours, consult a doctor.

Directions

Apply to hands until thoroughly wet.  Rub vigorously until dry.

Inactive Ingredients

Water (Aqua), Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Extract, Fragrance (Parfum), Triethanolamine, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate (Vitamin A)

Package Labeling:

Label

Package Labeling:240ml

Box

Package Labeling:500ml

Box2

ALOE VERA LEAF HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 74856-024
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
TROLAMINE (UNII: 9O3K93S3TK)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
VITAMIN A (UNII: 81G40H8B0T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 74856-024-0060 mL in 1 BOTTLE; Type 0: Not a Combination Product06/08/202003/01/2021
2NDC: 74856-024-01240 mL in 1 BOTTLE; Type 0: Not a Combination Product08/31/202003/01/2021
3NDC: 74856-024-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product08/31/202003/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/08/202003/01/2021
Labeler - UI Global Brands LLC (049073416)

Revised: 12/2022
 

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