Theochem Foaming Hand Sanitizer

Manufacturer
Theochem Laboratories Inc
Effective date
2013-06-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:37:50

Label at a glance#

ProductTheochem Foaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

- For hand sanitizing to decrease bacteria on the skin. - Recommended for repeated use.

Dosage and administration

- Pump a small amount of foam into palm of hand. - Rub throughly over all surfaces of both hands. - Rub hands together briskly until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

- For hand sanitizing to decrease bacteria on the skin.

- Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

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 right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

- Pump a small amount of foam into palm of hand.

- Rub throughly over all surfaces of both hands.

- Rub hands together briskly until dry.

Other Information

OTHER SAFETY INFORMATION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, dihydroxypropyl PEG-5 linoleammonium chloride, glycereteh-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide.

PRINCIPAL DISPLAY PANEL- 1250 ml FOAMING HAND SANITIZERNet Contents: 1250 ml.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANELPACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN1
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD1
1038799benzalkonium chloride 0.1 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68878-118-102019-11-27C16284748780-19855e2a2-4c86-60a7-e053-dbdaa90a05bdFoaming Hand Santizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68878-118-10Theochem Foaming Hand Sanitizer1250 mL in 1 BOTTLE, DISPENSINGLIQUID12501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68878-118THEOCHEM FOAMING HAND SANITIZER (FOAMING HAND SANTIZER) LIQUID [THEOCHEM LABORATORIES INC]1Legacy NDC, 1 package rows20131218_3da40799-9a82-4a8d-b9ed-46e838952c48.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W71
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68878-11868878-118-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT

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
4c10210c-8cff-4931-a507-bb01e8d5003e3da40799-9a82-4a8d-b9ed-46e838952c482013-06-20WarningsExact identifier
spl id: 4c10210c-8cff-4931-a507-bb01e8d5003e
spl set id: 3da40799-9a82-4a8d-b9ed-46e838952c48

Reported adverse events (FAERS/openFDA)#

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