Adventure First Aid .5 Tin

Manufacturer
Tender Corporation
Effective date
2017-03-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:49:16

Label at a glance#

ProductAdventure First Aid .5 Tin
Active ingredientBENZOCAINE, ALCOHOL, ISOPROPYL ALCOHOL, BENZALKONIUM CHLORIDE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, BACITRACIN ZINC
Label structure17 sections

Dosage and administration

For External use only. Keep out of Reach of Children. Stop use if unusual redness, swelling or other symptoms occur, consult a physician immediately. Do not uses in eyes or over large areas of the body. Tear open packet, unfold towelette and use to cleanse desired skin area. Discard towelette appropriately after single use.

Label contents#

Full prescribing information#

Active Ingredient - Antiseptic

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose - Antiseptic

OTC - PURPOSE SECTION

Antiseptic

Use - Antiseptic

INDICATIONS & USAGE SECTION

For Professional and hospital use. Helps prevent infection. Antiseptic cleansing of face, hands and body without soap and water.

Warnings, Precautions and Directions - Antiseptic

WARNINGS SECTION

For External use only.

Keep out of Reach of Children.

Stop use if unusual redness, swelling or other symptoms occur, consult a physician immediately.

Do not uses in eyes or over large areas of the body.

Tear open packet, unfold towelette and use to cleanse desired skin area. Discard towelette appropriately after single use.

Inactive Ingredients - Antiseptic

INACTIVE INGREDIENT SECTION

Purified Water

Active Ingredient - Alcohol Prep Pad

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%

Use - Alcohol Prep Pad

INDICATIONS & USAGE SECTION

For preparation of the skin before injection

Warnings, Precautions and Directions - Alcohol Prep Pad

DOSAGE & ADMINISTRATION SECTION

For External Use Only

Flammable - Keep away from fire or flame

Do Not Use - with electrocautery, in eyes

Stop Use and Ask a Doctor if - Irritation or redness develop and persists for more than 72 hours

Keep out of Reach of Children

If swallowed, get medical help or contact a poison control center right away.

Tear Open packet, unfold and use as and wipe injection site vigorously and discard.

Store at Room Temperature

Active Ingredients - Insect Relief Pad

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 6%

SD alcohol 60%

Purpose - Insect Relief Pad

OTC - PURPOSE SECTION

Topical Anesthetic - Antiseptic

Use - Insect Relief Pad

INDICATIONS & USAGE SECTION

For the temporary relief of pain and itching associated with minor burns, scrapes and insect bites

Warnings, Precautions and Directions - Insect Relief Pad

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Clean intended area thoroughly with pad. Discard after single use

Warnings: For external use only.

Avoid contact with eyes. If this happens, rinse thoroughly with water

If swallowed, get medical help or contact a Poison Control Center right away

Flammable - keep away from fire or flame

Do not use: In eyes, on broken skin, deep puncture wounds. If unusual redness, swelling, irritation or other symptoms occur, consult a physician immediately.

Active Ingredients - Triple Antibiotic Ointment

OTC - ACTIVE INGREDIENT SECTION

Bacitracin Zinc 400 units

Neomycin Sulfate 5mg ( equivalent to 3.5 mg Neomycin base)

Polymyxin B Sulfate 5000 units

Purpose - Triple Antibiotic Ointment

OTC - PURPOSE SECTION

Triple Antibiotic

Use - Triple Antibiotic Ointment

INDICATIONS & USAGE SECTION

To help prevent infection in: minor cuts; scrapes and burns

Warnings, Precautions and Directions - Triple Antibiotic Ointment

WARNINGS SECTION

For external use only.

Do not use: in eyes; over large areas of the body;

If allergic to any of the ingredients; for more than one week unless directed by a physician

Stop use and consult a doctor: if the condition persists or gets worse; a rash or other allergic reaction develops.

Keep out of reach of children.

If ingested, contact a Poison Control Center right away

Directions: clean affected area; apply small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily; may be covered with a sterile bandage.

Adventure First Aid .5 Tin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Triple Antibiotic OintmentTriple Antibiotic OintmentHangtagHangtagHangtagHangtagAlcohol PadAlcohol PadISRPISRPAntiseptic WipeAntiseptic Wipe

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
204602bacitracin 400 UNT / neomycin 3.5 MG / polymyxin B 5000 UNT per GM Topical OintmentPSN1
1046313benzocaine 6 % / ethanol 60 % Medicated PadPSN1
797544isopropyl alcohol 70 % Medicated PadPSN1
204602bacitracin 0.4 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 5 UNT/MG Topical OintmentSCD1
1046313benzocaine 60 MG/ML / ethanol 0.6 ML/ML Medicated PadSCD1
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD1
204602bacitracin 400 UNT / neomycin 3.5 MG (as neomycin sulfate 5 MG) / polymyxin B 5000 UNT per GM Topical OintmentSY1
1046313benzocaine 6 % / ethanol 60 % Topical SwabSY1
797544isopropyl alcohol 70 % Medicated PadSY1
797544isopropyl alcohol 70 % Topical ClothSY1
797544isopropyl alcohol 70 % Topical SwabSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
BACITRACIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
BENZOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
NEOMYCIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
POLYMYXIN B Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130707708102004GTIN-13: 0707708102004
EAN-13: 0707708102004
GTIN-12: 707708102004
UPC-A: 707708102004
GTIN storage (14 digits): 00707708102004
4120-0200_AFA_Water Resistant_Hang Tag_Page_1.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
99e684e6-f435-feb8-d2bb-3a546f1cb768Product name220161117
25340b3b-3e4c-4ff8-abf6-3e62ec46bd0cProduct name120160603
2d352c73-a357-4193-a4de-dfdf9a2ac8e4Product name120150819
b045ad64-0f28-9a02-2f9b-b34d94fb2278Product name120140508
b6082387-f592-1148-0844-bd068fd213fbProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44224-0203-12023-01-30C16284748780-1f386c64a-25b8-0266-e053-dadaa90a7c1aAdventure First Aid .5 Tin

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44224-0203-1Adventure First Aid .5 Tin1 in 1 BOXKIT11
52124-0001-1Adventure First Aid .5 Tin0.8 mL in 1 PACKAGESWAB3 mL in .81.3 mg in 1mL1
52124-0008-1Adventure First Aid .5 Tin0.5 mL in 1 PACKAGESWAB1 mL in .560 mL in 100mL1
52124-0017-1Adventure First Aid .5 Tin0.7 mL in 1 PACKAGESWAB3 mL in .7700 mg in 1mL1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44224-0203ADVENTURE FIRST AID .5 TIN (BENZOCAINE, ALCOHOL, BENZALKONIUM CHLORIDE) KIT [TENDER CORPORATION]1Legacy NDC, 4 package rows20170316_4ad9d0a5-cd17-0808-e054-00144ff8d46c.zip
52124-0001ADVENTURE FIRST AID .5 TIN (BENZOCAINE, ALCOHOL, BENZALKONIUM CHLORIDE) KIT [TENDER CORPORATION]1Legacy NDC20170316_4ad9d0a5-cd17-0808-e054-00144ff8d46c.zip
52124-0003ADVENTURE FIRST AID .5 TIN (BENZOCAINE, ALCOHOL, BENZALKONIUM CHLORIDE) KIT [TENDER CORPORATION]1Legacy NDC20170316_4ad9d0a5-cd17-0808-e054-00144ff8d46c.zip
52124-0008ADVENTURE FIRST AID .5 TIN (BENZOCAINE, ALCOHOL, BENZALKONIUM CHLORIDE) KIT [TENDER CORPORATION]1Legacy NDC20170316_4ad9d0a5-cd17-0808-e054-00144ff8d46c.zip
52124-0017ADVENTURE FIRST AID .5 TIN (BENZOCAINE, ALCOHOL, BENZALKONIUM CHLORIDE) KIT [TENDER CORPORATION]1Unmatched20170316_4ad9d0a5-cd17-0808-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
4ad9d0a5-cd18-0808-e054-00144ff8d46c4ad9d0a5-cd17-0808-e054-00144ff8d46c2017-03-16WarningsExact identifier
spl id: 4ad9d0a5-cd18-0808-e054-00144ff8d46c
spl set id: 4ad9d0a5-cd17-0808-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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