FDA.reportPublic FDA data

Germs be gone Sanitizer

Manufacturer
Brands International Corporation
Effective date
2021-08-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:41:55

Label at a glance#

ProductGerms be gone Sanitizer Scented
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Adults and children over 2 years: For occasional and personal domestic use Supervise children when they use this product rub thoroughly into hands for at least 30 seconds. Allow to dry.

Storage and handling

Store between 15-30C (59-86F). Avoid freezing and excessive heat above 40C (104F) may discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic skin cleanser

Use

INDICATIONS & USAGE SECTION

Effective in destroying harmful bacteria to provide antiseptic cleaning

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

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

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 2 years: For occasional and personal domestic use Supervise children when they use this product rub
thoroughly into hands for at least 30 seconds. Allow to dry.

Other information

STORAGE AND HANDLING SECTION

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

may discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water), Lauramine oxide, Glycerin, Cetrimonium Chloride, Vitamin E (Tocopherol), Aloe Barbadensis Leaf Extract, DMDM Hydantoin

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

66

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN2
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD2
1020365benzalkonium chloride 0.13 % Topical FoamSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50157-526-232025-01-30C16284748780-12cef2736-8d61-d83d-e063-dadaa90ab31fGerms be Gone Foam sanitizer - Scented

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50157-526-23Germs be gone SanitizerScented236 mL in 1 BOTTLE, PUMPSOLUTION2362

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50157-526GERMS BE GONE SANITIZER SCENTED (HAND SANITIZER) SOLUTION [BRANDS INTERNATIONAL CORPORATION]2Legacy NDC, 1 package rows20210816_c99098e1-3a1f-22d2-e053-2a95a90a2c8d.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50157-52650157-526-23

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALOEV5VD430YW9IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
DMDM HYDANTOINBYR0546TOWIACT
LAURAMINE OXIDE4F6FC4MI8WIACT

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
c991074f-9d95-6592-e053-2a95a90a8c08c99098e1-3a1f-22d2-e053-2a95a90a2c8d2021-08-14WarningsExact identifier
spl id: c991074f-9d95-6592-e053-2a95a90a8c08
spl set id: c99098e1-3a1f-22d2-e053-2a95a90a2c8d

Reported adverse events (FAERS/openFDA)#

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