Relief C Hand Sanitizer Unscented for Professionals

Manufacturer: FGD, LLC | Goodwin Co.
Effective date: 2021-01-06
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-05-31 23:36:33

Label at a glance#

ProductRelief C Hand Sanitizer Unscented for Professionals

Active ingredientALCOHOL

Label structure12 sections

Indications and uses

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

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

OTC - DO NOT USE SECTION

on children less than 2 months of age
on open skin wounds

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

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 hit produce to avoid swallowing.

OTHER SAFETY INFORMATION

Store between 15-30 ^oC (59-86 ^oF)
Avoid freezing and excessive heat 40 ^oC (104 ^oF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, PEG-6 (and) AMP-Acrylate/vinyl-Isodecanoate Crosspolymer, Propylene-glycol, Purified Water

Relief C Hand Sanitizer Unscented for Professionals 8 oz jaguar

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

relief.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	4
581662	ethanol 0.7 ML/ML Topical Gel	SCD	4
581662	ethanol 70 % Topical Gel	SY	4
581662	ethyl alcohol 70 % Topical Gel	SY	4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73787-120-01	2023-01-30	C162847	48780-1	f386c649-b42d-0266-e053-dadaa90a7c1a	Relief C Hand Sanitizer Unscented for Professionals 8 oz jaguar

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73787-120-01	Relief C Hand Sanitizer Unscented for Professionals	236 mL in 1 BOTTLE	GEL	236		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73787-120	RELIEF C HAND SANITIZER UNSCENTED FOR PROFESSIONALS (ETHYL ALCOHOL) GEL [FGD, LLC]	4	Legacy NDC, 1 package rows	20210107_a7d7f966-0ea3-7c86-e053-2995a90a50bf.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Relief C Hand Sanitizer Unscented for Professionals
Ethyl Alcohol
CITRIC ACID MONOHYDRATE
WATER
GUARAPROLOSE (1300 MPA.S AT 1%)
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73787-120	73787-120-01

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
Name	UNII	Kind
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
WATER	059QF0KO0R	IACT
GUARAPROLOSE (1300 MPA.S AT 1%)	1530WMS90S	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
b8405df8-a0be-4951-e053-2a95a90abcfd			a7d7f966-0ea3-7c86-e053-2995a90a50bf	2021-01-06	Warnings	Exact identifier spl id: b8405df8-a0be-4951-e053-2a95a90abcfd spl set id: a7d7f966-0ea3-7c86-e053-2995a90a50bf

Reported adverse events (FAERS/openFDA)#

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