Germs Be Gone Hand Sanitizer

Manufacturer: Brands International
Effective date: 2020-05-16
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:13:31

Label at a glance#

ProductGerms Be Gone Hand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Indications and uses

helps reduce bacteria on the skin that could cause disease Recommended for repeated use

Dosage and administration

Place enough product in your palm to thoroughly cover your hands Rub hands together briskly until dry Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 80% w/w

Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Safety Instructions

OTHER SAFETY INFORMATION

Flammable, Keep away from fire and flame

Ask Doctor

OTC - ASK DOCTOR SECTION

Stop Use and Ask a doctor if irritation or redness develops

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Other Information

OTHER SAFETY INFORMATION

Store below 110°F (43°C)
May discolor certain fabrics or surfaces.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

water, isopropyl alcohol, glycerin, carbomer, aminomethyl propanol, fragrance, propylene glycol, Aloe, Tocopheryl Acetate. isopropyl myristate

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm to thoroughly cover your hands
Rub hands together briskly until dry
Children under 6 years of age should be supervised when using this product.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame.

Uses

INDICATIONS & USAGE SECTION

helps reduce bacteria on the skin that could cause disease
Recommended for repeated use

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC:

50157-503-01: 118ml

50157-503-02: 148ml

50157-503-05: 148ml : Bottle, Spray

50157-503-03: 236ml

50157-503-04: 443ml

IMG_1688

14oz

4oz

5oz

8oz

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1041498	ethanol 80 % Topical Gel	PSN	3
1041498	ethanol 0.8 ML/ML Topical Gel	SCD	3
1041498	ethanol 80 % Topical Gel	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
50157-503-01	2025-01-30	C162847	48780-1	2cef2736-78f4-d83d-e063-dadaa90ab31f	Germs be gone Hand Sanitizer
50157-503-02	2025-01-30	C162847	48780-1	2cef2736-78f4-d83d-e063-dadaa90ab31f	Germs be gone Hand Sanitizer
50157-503-03	2025-01-30	C162847	48780-1	2cef2736-78f4-d83d-e063-dadaa90ab31f	Germs be gone Hand Sanitizer
50157-503-04	2025-01-30	C162847	48780-1	2cef2736-78f4-d83d-e063-dadaa90ab31f	Germs be gone Hand Sanitizer
50157-503-05	2025-01-30	C162847	48780-1	2cef2736-78f4-d83d-e063-dadaa90ab31f	Germs be gone Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
50157-503-01	Germs Be Gone Hand Sanitizer	118 mL in 1 BOTTLE	GEL	118	3
50157-503-02	Germs Be Gone Hand Sanitizer	148 mL in 1 BOTTLE	GEL	148	3
50157-503-03	Germs Be Gone Hand Sanitizer	236 mL in 1 BOTTLE	GEL	236	3
50157-503-04	Germs Be Gone Hand Sanitizer	443 mL in 1 BOTTLE	GEL	443	3
50157-503-05	Germs Be Gone Hand Sanitizer	148 mL in 1 BOTTLE, SPRAY	GEL	148	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50157-503	GERMS BE GONE HAND SANITIZER (ETHYL ALCOHOL) GEL [BRANDS INTERNATIONAL]	3	Legacy NDC, 5 package rows	20200518_b97a38cf-a426-4274-ac48-4ed0a9249db1.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Germs Be Gone Hand Sanitizer
Ethyl Alcohol
WATER
ISOPROPYL ALCOHOL
ISOPROPYL MYRISTATE
ALOE VERA LEAF
PROPYLENE GLYCOL
GLYCERIN
CARBOMER COPOLYMER TYPE A
.ALPHA.-TOCOPHEROL ACETATE, D-
AMINOMETHYLPROPANOL
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50157-503	50157-503-01, 50157-503-02, 50157-503-03, 50157-503-04, 50157-503-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER COPOLYMER TYPE A	71DD5V995L	IACT
.ALPHA.-TOCOPHEROL ACETATE, D-	A7E6112E4N	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a5c69c86-e43f-358a-e053-2a95a90a0950			b97a38cf-a426-4274-ac48-4ed0a9249db1	2020-05-16	Warnings	Exact identifier spl id: a5c69c86-e43f-358a-e053-2a95a90a0950 spl set id: b97a38cf-a426-4274-ac48-4ed0a9249db1

Reported adverse events (FAERS/openFDA)#

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