Hand Sanitizer

Manufacturer
MCRL Overseas Printing Inc | Huizhou Bliss Commodity Co. Ltd
Effective date
2020-04-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:07:57

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Put a thumb size amount in your palm and rub hands together briskly until dry. Other information: do not store in temperature over 118F. children under the 6 years of age should be supervised while using this product. may discolor certain fabrics.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Sanitizer

Use

INDICATIONS & USAGE SECTION

  • to decrease bacterias on the skin that could cause diseases.
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only-hands. Use only as directed. Excessive use or prolonged exposure may cause irritation to skin. Discontinue use if rash, redness or itching appears. Flammable. Keep away from heat or flame.

When using this product

  • keep out of eyes. In case of contact with eyes, immediately flush with water and call a doctor. 
  • avoid contact with broken skin.

Stop use and ask a doctor if irritation or redness develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion seek professional assistance or contact a poison control center immedietly.

Directions

DOSAGE & ADMINISTRATION SECTION

Put a thumb size amount in your palm and rub hands together briskly until dry.

Other information:

  • do not store in temperature over 118F.
  • children under the 6 years of age should be supervised while using this product.
  • may discolor certain fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, glycerin, propylene Glycol, carbomer, sodium hydroxide

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 1

Label 1Label 1

Label 2

Label 2Label 2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76626-002-012024-07-30C16284748780-11030e365-45f4-111a-e063-dadaa90a10e2cc8a2ffb-ef43-41f0-a503-0596577644c9
76626-002-022024-07-30C16284748780-11030e365-45f4-111a-e063-dadaa90a10e2cc8a2ffb-ef43-41f0-a503-0596577644c9
76626-002-032024-07-30C16284748780-11030e365-45f4-111a-e063-dadaa90a10e2cc8a2ffb-ef43-41f0-a503-0596577644c9
76626-002-042024-07-30C16284748780-11030e365-45f4-111a-e063-dadaa90a10e2cc8a2ffb-ef43-41f0-a503-0596577644c9
76626-002-052024-07-30C16284748780-11030e365-45f4-111a-e063-dadaa90a10e2cc8a2ffb-ef43-41f0-a503-0596577644c9
76626-002-062024-07-30C16284748780-11030e365-45f4-111a-e063-dadaa90a10e2cc8a2ffb-ef43-41f0-a503-0596577644c9
76626-002-072024-07-30C16284748780-11030e365-45f4-111a-e063-dadaa90a10e2cc8a2ffb-ef43-41f0-a503-0596577644c9
76626-002-012024-01-30C16284748780-11030e365-45f4-111a-e063-dadaa90a10e2cc8a2ffb-ef43-41f0-a503-0596577644c9
76626-002-022024-01-30C16284748780-11030e365-45f4-111a-e063-dadaa90a10e2cc8a2ffb-ef43-41f0-a503-0596577644c9
76626-002-032024-01-30C16284748780-11030e365-45f4-111a-e063-dadaa90a10e2cc8a2ffb-ef43-41f0-a503-0596577644c9
76626-002-042024-01-30C16284748780-11030e365-45f4-111a-e063-dadaa90a10e2cc8a2ffb-ef43-41f0-a503-0596577644c9
76626-002-052024-01-30C16284748780-11030e365-45f4-111a-e063-dadaa90a10e2cc8a2ffb-ef43-41f0-a503-0596577644c9
76626-002-062024-01-30C16284748780-11030e365-45f4-111a-e063-dadaa90a10e2cc8a2ffb-ef43-41f0-a503-0596577644c9
76626-002-072024-01-30C16284748780-11030e365-45f4-111a-e063-dadaa90a10e2cc8a2ffb-ef43-41f0-a503-0596577644c9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76626-002-01Hand Sanitizer30 mL in 1 BOTTLE, PLASTICGEL301
76626-002-02Hand Sanitizer60 mL in 1 BOTTLE, PLASTICGEL601
76626-002-03Hand Sanitizer237 mL in 1 BOTTLE, PLASTICGEL2371
76626-002-04Hand Sanitizer100 mL in 1 BOTTLE, PLASTICGEL1001
76626-002-05Hand Sanitizer300 mL in 1 BOTTLE, PLASTICGEL3001
76626-002-06Hand Sanitizer500 mL in 1 BOTTLE, PLASTICGEL5001
76626-002-07Hand Sanitizer1000 mL in 1 BOTTLE, PLASTICGEL10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76626-002HAND SANITIZER (ALCOHOL) GEL [MCRL OVERSEAS PRINTING INC]1Legacy NDC, 7 package rows20200425_cc8a2ffb-ef43-41f0-a503-0596577644c9.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76626-00276626-002-01, 76626-002-02, 76626-002-03, 76626-002-04, 76626-002-05, 76626-002-06, 76626-002-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML · Source PDF

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
e1a51e29-2a33-4a60-8c07-aa370395f6b3cc8a2ffb-ef43-41f0-a503-0596577644c92020-04-23WarningsExact identifier
spl id: e1a51e29-2a33-4a60-8c07-aa370395f6b3
spl set id: cc8a2ffb-ef43-41f0-a503-0596577644c9

Reported adverse events (FAERS/openFDA)#

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