FDA.reportPublic FDA data

Compound Benzoin Tincture Label

Manufacturer
Medical Chemical Corporation
Effective date
2026-07-01
Label type
HUMAN OTC DRUG LABEL
Version
19
Source
weekly-update
Hydrated at
2026-07-17 21:43:19

Label at a glance#

ProductCompound Benzoin Tincture
Active ingredientBENZOIN RESIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Aloe, Benzoin, Storax, Tolu Balsam, Ethanol

OTC - PURPOSE SECTION

Purpose: Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings: Keep out of reach of children.  Ingestion will result in severe gastrointestinal distress, unconsciousness and death.  If ingested induce vomiting if the victim is conscious.  Contact a poison control center immediately.

INDICATIONS & USAGE SECTION

Directions: Apply to affected area for first-aid treatment of minor cuts and abrasions.  Discontinue use and get medical aid if redness, irritation or infection develops.  In case of deep or puncture wounds consult a physician.

WARNINGS SECTION

Warnings: Keep out of reach of children.  Ingestion will result in a severe gastrointestinal distress, unconsciousness and death.  If ingested induce vomiting if victim is conscious.  Contact a poison control center immediately.

DOSAGE & ADMINISTRATION SECTION

Directions: Apply to affected area for first-aid treatment of minor cuts and abrasions.  Discontinue use and get medical aid if redness, irritation or infection develops.  In case of deep or puncture wounds consult a physician.

INACTIVE INGREDIENT SECTION

Enter section text here

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

benzoinlabel.jpg

Compound Benzoin Tincture LabelCompound Benzoin Tincture Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
12745-109-012024-01-30C16284748780-11030e365-4283-111a-e063-dadaa90a10e2Compound Benzoin Tincture Label
12745-109-012024-01-30C16284748780-11030e365-4283-111a-e063-dadaa90a10e2Compound Benzoin Tincture Label
12745-109-022024-01-30C16284748780-11030e365-4283-111a-e063-dadaa90a10e2Compound Benzoin Tincture Label
12745-109-022024-01-30C16284748780-11030e365-4283-111a-e063-dadaa90a10e2Compound Benzoin Tincture Label
12745-109-032024-01-30C16284748780-11030e365-4283-111a-e063-dadaa90a10e2Compound Benzoin Tincture Label
12745-109-032024-01-30C16284748780-11030e365-4283-111a-e063-dadaa90a10e2Compound Benzoin Tincture Label
12745-109-042024-01-30C16284748780-11030e365-4283-111a-e063-dadaa90a10e2Compound Benzoin Tincture Label
12745-109-042024-01-30C16284748780-11030e365-4283-111a-e063-dadaa90a10e2Compound Benzoin Tincture Label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZOIN RESINACTIVE INGREDIENTGK21SBA74R9
BENZOIN RESINACTIVE MOIETYGK21SBA74R9
WATERINACTIVE INGREDIENT059QF0KO0R9

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
12745-10912745-109-01, 12745-109-02, 12745-109-03, 12745-109-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BENZOIN RESINGK21SBA74RACTIB

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
182025-07-31full-release2026-06-01 01:12:01

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
Compound Benzoin TinctureTINCTURE OF BENZOINMedical Chemical Corporation243494ee-342d-4c32-9a86-f8c6c347bd8b2026-07-01WarningsExact identifier
ndc (package): 12745-109-04
ndc (package): 12745-109-02
ndc (package): 12745-109-01
ndc (package): 12745-109-03
ndc (product): 12745-109
ndc11 (package): 12745010904
ndc11 (package): 12745010903
ndc11 (package): 12745010902
ndc11 (package): 12745010901
spl id: 55933c46-b6ef-7902-e063-6394a90a61c7
spl set id: 243494ee-342d-4c32-9a86-f8c6c347bd8b

Reported adverse events (FAERS/openFDA)#

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