FDA.reportPublic FDA data

BAC-D Antibacterial Wound and Skin care

Manufacturer
RDM Products, Inc
Effective date
2015-11-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:44:01

Label at a glance#

ProductBAC-D Antibacterial Wound and Skin care
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

First aid to help prevent the risk of bacterial contamination in minor cuts, scrapes, burns and post-surgical incision sites.

Dosage and administration

Clean the affected area Spray a small amount of this product on the area 1 to 3 times a day. May be covered with a sterile  bandage If bandaged let dry first

Label contents#

Full prescribing information#

Active ingredient 

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13 %

Purpose

OTC - PURPOSE SECTION

First aid Product

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.

Uses

INDICATIONS & USAGE SECTION

First aid to help prevent the risk of bacterial contamination in minor cuts, scrapes, burns and post-surgical incision sites.

Warnings

WARNINGS SECTION

For external use only. 

Do not use

  • in the eyes or apply over large areas of the body  longer than 1 week unless directed by a doctor

Directions for use

DOSAGE & ADMINISTRATION SECTION

  • Clean the affected area
  • Spray a small amount of this product on the area 1 to 3 times a day.
  • May be covered with a sterile  bandage
  • If bandaged let dry first

Inactive ingredients 

INACTIVE INGREDIENT SECTION

Ionized water, Carbamide

SPL UNCLASSIFIED SECTION

Made in the U.S.A 

Manufactured for 

RDM Products Inc.

910-491-7371

PO Box 35003

Fayetteville, NC 28303

www.BAC-D.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AnimalSprayAnimalSpray

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039012benzalkonium chloride 0.13 % Topical SprayPSN2
1039012benzalkonium chloride 1.3 MG/ML Topical SpraySCD2
1039012benzalkonium chloride 0.13 % Topical SpraySY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69082-500-042020-01-31C16284748780-19d75b9d0-8035-f424-e053-dadaa90a57ceBAC-D Antibacterial Wound and Skin care

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69082-500-04BAC-D Antibacterial Wound and Skin care118 mL in 1 BOTTLESPRAY1182

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69082-500BAC-D ANTIBACTERIAL WOUND AND SKIN CARE (BENZALKONIUM CHLORIDE) SPRAY [RDM PRODUCTS, INC]2Legacy NDC, 1 package rows20151111_6781cf5e-b310-4124-8e35-d2208cf1eb55.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W72
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y2
UREAINACTIVE INGREDIENT8W8T17847W2
WATERINACTIVE INGREDIENT059QF0KO0R2

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
69082-50069082-500-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
UREA8W8T17847WIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 7 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
UREAUREA8W8T17847WTABLET, EFFERVESCENT / ORAL60 mgExact identifier — unii candidate
7 equally ranked IID candidates
UREAUREA8W8T17847WINSERT / VAGINAL50 mgExact identifier — unii candidate
7 equally ranked IID candidates
UREAUREA8W8T17847WCREAM / VAGINAL0.64 %w/wExact identifier — unii candidate
7 equally ranked IID candidates
UREAUREA8W8T17847WTABLET, EXTENDED RELEASE / ORAL0.01 mgExact identifier — unii candidate
7 equally ranked IID candidates
UREAUREA8W8T17847WSYSTEM / TOPICAL840 mgExact identifier — unii candidate
7 equally ranked IID candidates
UREAUREA8W8T17847WTABLET, COATED / ORAL0.02 mgExact identifier — unii candidate
7 equally ranked IID candidates
UREAUREA8W8T17847WDOUCHE / VAGINAL8 %w/wExact identifier — unii candidate
7 equally ranked IID candidates

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
ac4016b2-8a98-47d8-a2ef-c3a387f876146781cf5e-b310-4124-8e35-d2208cf1eb552015-11-10WarningsExact identifier
spl id: ac4016b2-8a98-47d8-a2ef-c3a387f87614
spl set id: 6781cf5e-b310-4124-8e35-d2208cf1eb55

Reported adverse events (FAERS/openFDA)#

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