Relief C Hand Sanitizer Unscented for Professionals

Manufacturer
FGD, LLC | Goodwin Co.
Effective date
2021-01-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:36:32

Label at a glance#

ProductRelief C Hand Sanitizer Unscented for Professionals
Active ingredientALCOHOL
Label structure13 sections

Indications and uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Highly flammable liquid and vapor. Causes serious eye irritation. Keep away from heat or flame.

Do Not Use

OTC - DO NOT USE SECTION

  • If you are allergic to any of the ingredients
  • In children less than 2 months of age
  • On open skin wounds

When using this product

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears and mouth.

In case of contact with eyes, rinse eyes thoroughly with water.

Stop use or ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

PRECAUTIONS SECTION

  • Keep away from heat/sparks/open flame/hot surfaces.
  • No Smoking. Keep container tightly closed and store in a well-ventilated place.
  • Avoid breathing vapors/mist/spray.
  • Contaminated work clothing should not be allowed out of the workplace.
  • Wear protective eye protection/face protection.
  • Dispose of contents/container to a licensed treatment, storage or disposal facility (TSRF)
  • If in eyes rinse continuously with water for several minutes. Remove contact lenses if present and easy to do – continue rinsing.
  • In case of fire use CO2, Halon (if permitted), dry chemical, or foam for extinction.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

OTHER SAFETY INFORMATION

  • Store between 15-30 0C (59-86 0F)
  • Avoid freezing and excessive heat above 40 0C (104 0F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbapol 20, glycerin, proylene glycol, water

Relief C Hand Sanitizer: Unscented for Professionals

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73787-122-012023-01-30C16284748780-1f386c649-e3e8-0266-e053-dadaa90a7c1aRelief C Hand Sanitizer: Unscented for Professionals

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73787-122-01Relief C Hand Sanitizer Unscented for Professionals946353 mL in 1 DRUMGEL9463533

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73787-122RELIEF C HAND SANITIZER UNSCENTED FOR PROFESSIONALS (ETHYL ALCOHOL) GEL [FGD, LLC]3Legacy NDC, 1 package rows20210107_a79a960e-2c63-9cdb-e053-2a95a90a4939.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73787-12273787-122-01

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

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
b840d034-9986-3f0e-e053-2a95a90a53c6a79a960e-2c63-9cdb-e053-2a95a90a49392021-01-06WarningsExact identifier
spl id: b840d034-9986-3f0e-e053-2a95a90a53c6
spl set id: a79a960e-2c63-9cdb-e053-2a95a90a4939

Reported adverse events (FAERS/openFDA)#

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