FDA.reportPublic FDA data

Code All Clear Hand Sanitizer

Manufacturer
DEICING DEPOT
Effective date
2020-07-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:21:55

Label at a glance#

ProductCode All Clear Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

To decrease bacteria on the skin that could cause disease. Recommended for repeated use.

Dosage and administration

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

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

80% Ethyl Alcohol 

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

USES

INDICATIONS & USAGE SECTION

  • To decrease bacteria on the skin that could cause disease.
  • Recommended for repeated use.

WARNINGS

WARNINGS SECTION

- FOR EXTERNAL USE ONLY - HANDS. FLAMMABLE. KEEP AWAY FROM HEAT AND FLAME.

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

  • 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

OTC - STOP USE SECTION

if skin irritation develops.

KKEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • 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

SPL UNCLASSIFIED SECTION

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

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

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

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77780-000-002022-06-01C16284748780-1d6a99b39-c4b4-a426-e053-dadaa90af4c2Code All-Clear Hand Sanitizer
77780-000-002022-01-28C16284748780-1d6a99b39-c4b4-a426-e053-dadaa90af4c2Code All-Clear Hand Sanitizer

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77780-00077780-000-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e06506ea-62cf-e1a9-e053-2a95a90a51f31db48fa8-91e6-4b24-b2fd-3799b19914232022-06-01WarningsExact identifier
spl set id: 1db48fa8-91e6-4b24-b2fd-3799b1991423

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.