Hand Sanitizer Gumdrop by BASE4 Ventures, Inc Hand Sanitizer Gumdrop

Hand Sanitizer Gumdrop by

Drug Labeling and Warnings

Hand Sanitizer Gumdrop by is a Otc medication manufactured, distributed, or labeled by BASE4 Ventures, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER GUMDROP- alcohol gel 
BASE4 Ventures, Inc

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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Hand Sanitizer Gumdrop

Drug Facts

Active Ingredients

Alcohol 66%

Purpose

Antimicrobial

Uses

• hand sanitizer to help decrease bacteria on the skin.
• recommended for repeated use.

Warnings

• For external use only.
• Flammable.
• Keep away from heat and flame.

When using this product,

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

if redness or irritation develop and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a poison control center immediately.

Directions

• Rub dime sized amount between hands until dry
• Supervise children in the use of this product
• In the case of eye contact rinse eyes thoroughly with water

Other information

• Do not store above 105ºF.
• may discolor some fabrics.

Inactive ingredients:

Water, Glycerin, Propylene Glycol, Triethanolamine, Carbomer, Fragrance, Aloe Barbadensis Extract, Tocopherol.

Package Labeling:

HAND SANITIZER GUMDROP 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62651-024
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62651-024-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/15/2020	04/27/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/15/2020	04/27/2021

Labeler - BASE4 Ventures, Inc (137316126)

Revised: 4/2021

Document Id: c1353b68-ffb2-19d8-e053-2995a90acf34

34390-5

Set id: 69f9df26-2ded-4898-bfb2-739fcff142c1

Version: 2

Effective Time: 20210430