FDA.reportPublic FDA data

3 in 1 First Aid Wound Care

Manufacturer
Rite Aid Corporation
Effective date
2023-11-22
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:02:38

Label at a glance#

Product3 in 1 First Aid Wound Care
Active ingredientBENZETHONIUM CHLORIDE
Label structure8 sections

Indications and uses

First aid to help prevent the risk of bacterial contamination in minor cuts, scrapes and burns.

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 ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzethonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

First aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

First aid to help prevent the risk of bacterial contamination in minor cuts, scrapes and burns.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • in the eyes or apply over large areas of the body
  • longer than 1 week, unless directed by a doctor
  • for single patient use only

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or punture wounds, animal bites or serious burns

When using this product

OTC - WHEN USING SECTION

  • do not puncture or incinerate
  • contents under pressure

Stop use and consult a doctor if

OTC - STOP USE SECTION

  • condition persists or gets worse

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Directions

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

Other information

SPL UNCLASSIFIED SECTION

  • Store between 59° and 86° F (15° and 30° C).
  • See bottom of can for lot # and expiration date

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf extract (aloe vera), benzalkonium chloride, maltodextrin, purified water, sodium bicarbonate, sodium chloride

Questions?

OTC - QUESTIONS SECTION

1-888-547-5492

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1302737benzethonium chloride 0.13 % Topical SolutionPSN6
1302737benzethonium chloride 1.3 MG/ML Topical SolutionSCD6
1302737benzethonium chloride 0.13 % Topical SolutionSY6

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-5074-12021-12-04C16284748780-1c7ccaba7-24ae-fd44-e053-dadaa90aa01b3 in 1 First Aid Wound Care
11822-5074-12021-07-23C16284748780-1c7ccaba7-24ae-fd44-e053-dadaa90aa01b3 in 1 First Aid Wound Care

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-5074-13 in 1 First Aid Wound Care211 g in 1 BOTTLESOLUTION2116

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-50743 IN 1 FIRST AID WOUND CARE (BENZETHONIUM CHLORIDE) SOLUTION [RITE AID CORPORATION]6Current NDC, Legacy NDC, 1 package rows20231123_05f4a1fe-a7df-4826-8104-c26d21b0e79d.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11822-507411822-5074-1

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
ALOE VERA LEAFZY81Z83H0XIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
MALTODEXTRIN7CVR7L4A2DIACT
WATER059QF0KO0RIACT
SODIUM BICARBONATE8MDF5V39QOIACT
SODIUM CHLORIDE451W47IQ8XIACT
BENZETHONIUM CHLORIDEPH41D05744ACTIB

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
3 in 1 First Aid Wound CareBENZETHONIUM CHLORIDERite Aid Corporation05f4a1fe-a7df-4826-8104-c26d21b0e79d2023-11-22WarningsExact identifier
ndc (package): 11822-5074-1
ndc (product): 11822-5074
ndc11 (package): 11822507401
spl id: 0ac857cb-e589-343f-e063-6294a90a0e7f
spl set id: 05f4a1fe-a7df-4826-8104-c26d21b0e79d

Reported adverse events (FAERS/openFDA)#

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