Code All-Clear Hand Sanitizer

Code All Clear Hand Sanitizer by

Drug Labeling and Warnings

Code All Clear Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by DEICING DEPOT. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CODE ALL CLEAR HAND SANITIZER- alcohol liquid 
DEICING DEPOT

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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Code All-Clear Hand Sanitizer

ACTIVE INGREDIENTS

80% Ethyl Alcohol 

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 HEAT AND FLAME.

WHEN USING THIS PRODUCT

• Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• Avoid contact with broken skin.
• Do not inhale or ingest.

STOP USE AND ASK A DOCTOR

if skin irritation develops.

KKEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS

• Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision
• Not recommended for infants.

OTHER INFORMATION

• Do not store above 105°F.
• May discolor some fabrics. 
• Harmful to wood finishes and plastics.

INACTIVE INGREDIENTS

17- 18% Sterilized Water, 1.5% Glycerine, 0.2% Hydrogen Peroxide 34%, Less than 0.01% Bittering Agent.

Package Labeling:

CODE ALL CLEAR HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77780-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.8 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77780-000-00	3178.5 mL in 1 JUG; Type 0: Not a Combination Product	07/02/2020	05/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/02/2020	05/01/2022

Labeler - DEICING DEPOT (969354781)

Revised: 6/2022

Document Id: e06506ea-62cf-e1a9-e053-2a95a90a51f3

34390-5

Set id: 1db48fa8-91e6-4b24-b2fd-3799b1991423

Version: 3

Effective Time: 20220601