Astringent Solution

Manufacturer
First Nation Group
Effective date
2023-09-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:25:35

Label at a glance#

ProductAstringent Solution
Active ingredientCALCIUM ACETATE MONOHYDRATE, ALUMINUM SULFATE TETRADECAHYDRATE
Label structure12 sections

Storage and handling

Protect from excessive heat.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients (in each packet) Purpose

Aluminum sulfate tetradecahydrate, 1347 mg Astringent*
Calcium acetate monohydrate, 952 mg Astringent*

*When combined together in water, these ingredients form the
active ingredient aluminum acetate. See Directions.

INDICATIONS & USAGE SECTION

Uses

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

OTC - PURPOSE 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 SECTION

FOR EXTERNAL USE ONLY

OTC - WHEN USING SECTION

When using this product

  • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
  • 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.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Dissolve 1 to 3 packets in a pint (16 oz) of cool or warm water.
  • Stir until fully dissolved; do not strain or filter. The resulting mixture contains 0.16% (1 packet), 0.32% (2 packets), or 0.48% (3packets) aluminum acetate and is ready for 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.

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.

STORAGE AND HANDLING SECTION

Protect from excessive heat.

INACTIVE INGREDIENT SECTION

Dextrin

OTC - QUESTIONS SECTION

1-855-221-5332

Distributed by:

First Nation Group, LLC

Niceville, FL 32578

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81469-10181469-101-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 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
065c8f1c-af42-de27-e063-6394a90a2cd4048c4b03-1cf0-b724-e063-6294a90a1cad2023-09-27WarningsExact identifier
spl set id: 048c4b03-1cf0-b724-e063-6294a90a1cad

Reported adverse events (FAERS/openFDA)#

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