Zep Tranq Mdw AB Foam

Manufacturer
Zep Inc.
Effective date
2025-12-26
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:28:42

Label at a glance#

ProductZep Tranq Mdw AB Foam
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Indications and uses

For hand washing to decrease bacteria on skin.

Dosage and administration

Wet hands with water. Massage soap into hands and wrists, emphasizing back of hands, knuckles and cuticles. Rinse thoroughly and dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial Hand Wash

Uses

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on skin.

Warnings

WARNINGS SECTION

For external use only. Do not use in the eyes; if in eyes, rinse promptly and thoroughly with water.

When using this product

OTC - WHEN USING SECTION

  • Do not swallow.
  • If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately

Stop use and ask a doctor

OTC - STOP USE SECTION

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

Keep out of reach of children and pets

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets. Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands with water.
  • Massage soap into hands and wrists, emphasizing back of hands, knuckles and cuticles.
  • Rinse thoroughly and dry.

Other information

OTHER SAFETY INFORMATION

  • Store at 20 to 25°C (68 to 77°F).
  • Dispose in accordance with all applicable federal, state and local regulations.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cetrimonium Chloride, Lauryl/Myristyl Amidopropyl Amine Oxide, Glycerin, Di-PPG-2 Myreth-10 Adipate, Fragrance, Phenoxyethanol, Iodopropynyl Butylcarbamate, Methylisothiazolinone, Hexanediol, Tetrasodium Iminodisuccinate, Methylchloroisothiazolinone, Citric Acid, Blue 1, Yellow 5

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-877-I-BUY-ZEP (1-877-428-9937)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

387_3387387_3387

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN9
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD9
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY9
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66949-387-09Zep Tranq Mdw AB Foam3300 mL in 1 CASELIQUID33009
66949-387-24Zep Tranq Mdw AB Foam15140 mL in 1 CASELIQUID151409

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66949-38766949-387-09, 66949-387-24

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
Zep Tranq Mdw AB FoamBENZALKONIUM CHLORIDEZep Inc.5c3c1ab7-96a7-6ca5-e053-2991aa0af2b92025-12-26WarningsExact identifier
ndc (package): 66949-387-09
ndc (package): 66949-387-24
ndc (product): 66949-387
ndc11 (package): 66949038709
ndc11 (package): 66949038724
spl id: 46debcbb-acc0-3524-e063-6394a90a2522
spl set id: 5c3c1ab7-96a7-6ca5-e053-2991aa0af2b9

Reported adverse events (FAERS/openFDA)#

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