FDA.reportPublic FDA data

Swan 876.002/876AC

Manufacturer
Nice-Pak Products, LLC
Effective date
2026-09-22
Label type
HUMAN OTC DRUG LABEL
Version
17
Source
daily-update
Hydrated at
2026-09-25 02:01:13

Label at a glance#

ProductRubbing
Active ingredientALCOHOL
Label structure14 sections

Indications and uses

first aid to help prevent the risk of infection in: minor cuts scrapes burns

Dosage and administration

clean the affected area apply a small amount of this product on the affected area 1 to 3 times daily may be covered with a sterile bandage if bandaged, let dry first

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

first aid to help prevent the risk of infection in:

  • minor cuts
  • scrapes
  • burns

Warnings

WARNINGS SECTION

For external use only. If taken internally serious gastric disturbances will result. 

Flammable

OTHER SAFETY INFORMATION

keep away from fire or flame, heat, spark, electrical

Ask a doctor before use

OTC - ASK DOCTOR SECTION

for deep or puncture wounds, animal bites or serious burns

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes
  • do not inhale
  • do not apply over large areas of the body
  • do not use longer than 1 week

Stop use and ask 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

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

Caution

GENERAL PRECAUTIONS SECTION

Fumes can be acutely irriting to skin, eyes ad the respiratory system.  Do not apply to irritated skin or if excessive irritation develops.  Avoid getting  into the eyes or on mucous membranes.  Avoid inhaling this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • clean the affected area
  • apply a small amount of this product on the affected area 1 to 3 times daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first

Inactive ingredients

INACTIVE INGREDIENT SECTION

acetone, denatonium benzoate, methyl isobutyl ketone, water

Adverse reaction

ADVERSE REACTIONS SECTION

Distributed by: Vi-Jon, LLC

8515 Page Ave.

St. Louis, MO 63114

DSP-TN-21091   DSP-MO-20087

Pat. D675, 101

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0869-0876-43

swan ®

Ethyl Rubbing Alcohol

70% by volume

  • First Aid Antiseptic
  • For Rubbing & Massaging

Square bottle uses less plastic than a similarly sized round bottle

Recyclable (if available in your area)

WARNING FLAMMABLE - Keep away from heat, spark, electrical, fire or flame

CAUTION: DO not point at self or others; product will squirt when squeezed.

Use only in well-ventilated area; fumes can be harmful.

16 FL OZ (1 PT) 473 mL

image descriptionimage descriptionimage descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData MatrixL0003708BCmm02.jpg
Data codeData MatrixL0003708FEmm01.jpg

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0869-0876-43ML - Milliliter0869-087692db2ea7-120f-48cc-98b1-21f4eda5cf1d12017-08-11

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M1
ALCOHOLACTIVE MOIETY3K9958V90M1
ACETONEINACTIVE INGREDIENT1364PS73AF1
DENATONIUM BENZOATEINACTIVE INGREDIENT4YK5Z54AT21
METHYL ISOBUTYL KETONEINACTIVE INGREDIENTU5T7B88CNP1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0869-08760869-0876-43

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
ACETONE1364PS73AFIACT
DENATONIUM BENZOATE4YK5Z54AT2IACT
METHYL ISOBUTYL KETONEU5T7B88CNPIACT
WATER059QF0KO0RIACT

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
162026-03-12full-release2026-06-01 01:49:55

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 · 8 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
DENATONIUM BENZOATEDENATONIUM BENZOATE4YK5Z54AT2SOLUTION / TOPICALNAExact identifier — unii+route
6 equally ranked IID candidates
DENATONIUM BENZOATEDENATONIUM BENZOATE4YK5Z54AT2GEL / TOPICALNAExact identifier — unii+route
6 equally ranked IID candidates
DENATONIUM BENZOATEDENATONIUM BENZOATE4YK5Z54AT2SWAB / TOPICALNAExact identifier — unii+route
6 equally ranked IID candidates
ACETONEACETONE1364PS73AFTABLET, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
2 equally ranked IID candidates
DENATONIUM BENZOATEDENATONIUM BENZOATE4YK5Z54AT2SOLUTION / TOPICALNAExact identifier — unii+route
6 equally ranked IID candidates
ACETONEACETONE1364PS73AFTABLET, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
2 equally ranked IID candidates
DENATONIUM BENZOATEDENATONIUM BENZOATE4YK5Z54AT2GEL / TOPICALNAExact identifier — unii+route
6 equally ranked IID candidates
DENATONIUM BENZOATEDENATONIUM BENZOATE4YK5Z54AT2SWAB / TOPICALNAExact identifier — unii+route
6 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
4cd5b9f5-c313-acbc-e063-6394a90ae318247b044b-59ec-4562-86d4-4a14218488db2026-03-12Warnings, Adverse reactionsExact identifier
spl set id: 247b044b-59ec-4562-86d4-4a14218488db

Reported adverse events (FAERS/openFDA)#

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