DIBAR LABS Hand Sanitizer

DIBAR LABS Hand Sanitizer by

Drug Labeling and Warnings

DIBAR LABS Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by S.E.N.D. LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DIBAR LABS HAND SANITIZER- alcohol gel 
S.E.N.D. 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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DIBAR LABS Hand Sanitizer

Drug Facts

Active ingredients

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

• to decrease bacteria on the skin that could cause disease
• recommended for repeated use

Warnings

For external use only: hands

Flammable, keep away from fire or flame.

When using this product

• keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• avoid contact ith broken skin
• do not inhale or ingest

Stop use and ask a doctor if

• irritation and redness develop
• condition persist for more than 72 hours

Keep out of reach of children

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

Directions

• wet hands thoroughly ith product and allo to dry ithout iping
• for children under 6, use only under adult supervision
• not reommended for infants

Other information

• do not store above 105°F
• may discolor some fabrics
• harmful to ood finishes and plastics

Inactive ingredients

water, biopol plus, vitamin E oily acetate, triethanolamine, aloe vera aqueous extract.

Questions?

visit www.dibarlabs.com / Phone (281)-566-2682

Packge Labeling:

DIBAR LABS HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81500-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
TROLAMINE (UNII: 9O3K93S3TK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81500-010-01	236.5 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/11/2021	01/12/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/11/2021	01/12/2021

Labeler - S.E.N.D. LLC (113486262)

Revised: 12/2021

Document Id: d35d2bcd-725c-38a1-e053-2a95a90a9152

34390-5

Set id: ba49752a-083e-e13f-e053-2995a90adf78

Version: 2

Effective Time: 20211217

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