Twizzler Strawberry Hand Sanitizer by Taste Beauty LLC Drug Facts

Twizzler Strawberry Hand Sanitizer by

Drug Labeling and Warnings

Twizzler Strawberry Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Taste Beauty LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

TWIZZLER STRAWBERRY HAND SANITIZER- alcohol gel 
Taste Beauty 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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Drug Facts

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Use

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 fire and flames.

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 eyes thoroughly with water.

Stop use and ask a doctor if

  • Irritation and redness develop.

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 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

Water, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance, Triethanolamine, Aloe Barbadensis Extract, Tocopheryl Acetate (Vitamin E), FD&C Red No.403 (Cl 16035), D&C Red No.33 (Cl 17200).

Principal Display Panel – 30 mL Bottle Label

TWIST
TWIZZLERS

STRAWBERRY
HAND SANITIZER

1 FL OZ/30 mL

Principal Display Panel – 30 mL Bottle Label
TWIZZLER STRAWBERRY HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 74825-7022
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)  
Glycerin (UNII: PDC6A3C0OX)  
Carbomer Interpolymer Type A (Allyl Sucrose Crosslinked) (UNII: 59TL3WG5CO)  
Trolamine (UNII: 9O3K93S3TK)  
Aloe Vera Flower (UNII: 575DY8C1ER)  
.alpha.-tocopherol acetate (UNII: 9E8X80D2L0)  
D&C Red No. 33 (UNII: 9DBA0SBB0L)  
FD&C Red No. 40 (UNII: WZB9127XOA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 74825-7022-130 mL in 1 BOTTLE; Type 0: Not a Combination Product07/31/202007/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/31/202007/31/2020
Labeler - Taste Beauty LLC (080073601)

Revised: 2/2022
 

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