STERIWEB RX (as PLD) - OMNICIDE ANTIMICROBIAL GEL (69085-466-05)

Manufacturer
SteriWeb Medical, LLC
Effective date
2023-09-26
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-05-31 23:56:19

Label at a glance#

ProductOmnicide Antimicrobial
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections

Indications and uses

First aid to help treat, protect and prevent skin infection associated with minor cuts scrapes burns

Dosage and administration

adults and children 2 years and older: clean the affected area; apply a small amount on the area 1-3 times daily; may be covered with a sterile bandage (let dry first) children under 2 years: ask a doctor

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride   0.13% w/w

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

First aid to help treat, protect and prevent skin infection associated with

  • minor cuts
  • scrapes
  • burns

Warnings

WARNINGS SECTION

For external use only

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

When using this product

OTC - WHEN USING SECTION

  • Do not use in or near the eyes
  • Do not use if you have a history of allergy to any of the ingredients

Stop and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms persist for more than 7 days, or clear up and occur again within a few days.

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 2 years and older: clean the affected area; apply a small amount on the area 1-3 times daily; may be covered with a sterile bandage (let dry first)
  • children under 2 years: ask a doctor

Other information

SPL UNCLASSIFIED SECTION

Avoid excessive heat.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

USP Petrolatum, Water, Polihexanide (PHBM)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

omnicide30omnicide30

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1098199benzalkonium chloride 0.13 % Topical GelPSN7
1098199benzalkonium chloride 0.0013 MG/MG Topical GelSCD7
1098199benzalkonium chloride 0.13 % Topical GelSY7

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69085-466-052025-01-30C16284748780-12cef2736-937e-d83d-e063-dadaa90ab31fSTERIWEB RX (as PLD) - OMNICIDE ANTIMICROBIAL GEL (69085-466-05)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69085-466-05Omnicide Antimicrobial30 g in 1 TUBEGEL307

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69085-466OMNICIDE ANTIMICROBIAL (BENZALKONIUM CHLORIDE) GEL [STERIWEB MEDICAL, LLC]7Legacy NDC, 1 package rows20230927_fd16f21f-c152-4811-b57e-7c0c96b4aadb.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69085-46669085-466-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
0646c72c-ab44-dff6-e063-6394a90ae622fd16f21f-c152-4811-b57e-7c0c96b4aadb2023-09-26WarningsExact identifier
spl id: 0646c72c-ab44-dff6-e063-6394a90ae622
spl set id: fd16f21f-c152-4811-b57e-7c0c96b4aadb

Reported adverse events (FAERS/openFDA)#

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