ALUMINUM ACETATE ASTRINGENT SOLUTION

Label at a glance#

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (in each packet)

OTC - ACTIVE INGREDIENT SECTION

Aluminum acetate

(Each powder packet, when mixed in water and ready for use, provides the active ingredient aluminum acetate resulting from the reaction of calcium acetate 839 mg and aluminum sulfate 1191 mg.)

Purpose

OTC - PURPOSE SECTION

Astringent

Uses

INDICATIONS & USAGE SECTION

temporarily relieves minor skin irritations due to:

• poison ivy
• poison oak
• poison sumac
• insect bites
• athlete's foot
• rashes caused by soaps, detergents, cosmetics, or jewelry

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

• avoid contact with eyes
• do not cover compress or wet dressing with plastic to prevent evaporation
• in some skin conditions, soaking too long may overdry

OTC - STOP USE SECTION

Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• mix one, two, or three packets in 16 oz of water to obtain the following modified Burrow's Solution

Number of Packets	Dilution	% Aluminum acetate
one packet	1:40 dilution	0.14%
two packets	1:20 dilution	0.28%
three packets	1:13 dilution	0.42%

• do not strain or filter the solution
• can be used as a compress, wet dressing, or a soak

FOR USE AS A COMPRESS OR WET DRESSING: soak a clean, soft cloth in the solution apply cloth loosely to affected area for 15 to 30 minutes repeat as needed or as directed by a doctor discard solution after each use

FOR USE AS A SOAK: soak affected area for 15 to 30 minutes as needed, or as directed by a doctor repeat 3 times a day or as directed by a doctor discard solution after each use

Other information

STORAGE AND HANDLING SECTION

protect from excessive heat

Inactive ingredients

INACTIVE INGREDIENT SECTION

dextrin

Questions or comments?

OTC - QUESTIONS SECTION

1-888-EPIC-RX1

SPL UNCLASSIFIED SECTION

Distributed by:
TAGI Pharma
South Beloit, IL 61080

PRINCIPAL DISPLAY PANEL - 12 Powder Packets Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 51224-153-24

ALUMINUM ACETATE
ASTRINGENT SOLUTION

Soothing, Effective Relief of Minor Skin Irritations due to:

Poison Ivy
Athlete's Foot
Insect Bites
Rashes

tagi PHARMA

Manufactured by:
Epic Pharma, LLC
Laurelton, NY 11413

Made in USA

Distributed by:
TAGI Pharma
South Beloit, IL 61080

12 POWDER PACKETS

DailyMed Billing Units#

DailyMed Socrata Ingredients#

Products#

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

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

• Aluminum Acetate Astringent
• Calcium Acetate and Aluminum sulfate
• Calcium Acetate
• Calcium Cation
• Aluminum sulfate
• Aluminum sulfate anhydrous
• icodextrin

NDC Codes#

Ingredients#

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

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

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.

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.

Reported adverse events (FAERS/openFDA)#

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