UNI-SOL Herbal - Animal Science Products, Inc.

Manufacturer
Animal Science Products, Inc.
Effective date
2026-10-07
Label type
OTC ANIMAL DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-10-10 01:01:51

Label at a glance#

ProductUNI-SOL Herbal
Active ingredientSALIX ALBA BARK
Label structure7 sections

Indications and uses

For use in drinking water of poultry and swine as an aid in reducing pain, fever and inflammation.

Dosage and administration

Discomfort Mix 52 ml per 1000 Kg bodyweight into the feed or drinking water daily to provide the target dose of 25 mg Salicylate per Kg bodyweight. Manage Reactions to Infection or Injury First day - Mix 104 ml per 1000 Kg bodyweight into the feed or drinking water daily. Following days - Mix 65 ml per 1000 Kg bodyweight into the feed or drinking water daily.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salix alba Willow Extract 486 g/L

Purpose

OTC - PURPOSE SECTION

Analgesic, Antipyretic, and Anti-Inflammatory Liquid Concentrate for Drinking Water Solutions.

Uses

INDICATIONS & USAGE SECTION

For use in drinking water of poultry and swine as an aid in reducing pain, fever and inflammation.

Warnings

WARNINGS SECTION

• Not for use in lactating dairy cattle.
• Not for use in poultry producing eggs for human consumption.
• A withdrawal period of 24 hours is recommended in meat.
• Not for human use.
• Keep out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

Discomfort

Mix 52 ml per 1000 Kg bodyweight into the feed or drinking water daily to provide the target dose of 25 mg Salicylate per Kg bodyweight.

Manage Reactions to Infection or Injury

First day - Mix 104 ml per 1000 Kg bodyweight into the feed or drinking water daily.

Following days - Mix 65 ml per 1000 Kg bodyweight into the feed or drinking water daily.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Thymus vulgaris Extract, Disodium Phosphate, Monopotassium Phosphate, Artificial Coloring, and Water.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57932-01157932-011-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-06-10daily-update2026-06-12 05:10:05
12026-05-19daily-update2026-06-03 18:03:23

Reported adverse events (FAERS/openFDA)#

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