POD CONCENTRATE- ultra-concentrated, premium, moderate-foam teat dip concentrate powder

POD by

Drug Labeling and Warnings

POD by is a Animal medication manufactured, distributed, or labeled by DeVere Company, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INSTRUCTIONS FOR USE

Ultra-Concentrate, Premium, Moderate-Foam Teat Dip Concentrate

This product is a concentrated powder that when added to water makes an oxidizing teat dip. POD CONCENTRATE does not contain chlorine, iodine or any other halogens and is designed to clean and sanitize bovine teats before milking. This product works best on relatively clean teats and can be used after milking if environmental challenges are minimal.

Directions

Dilution

Dilute 2,2% of this products with water[e.g. 100lbs[4.5kg] of powder into 55gal [208L] water]

Pre-Milking use

Before milking, dip or spray entire teat with the diluted product. Wipe teats and udder dry after application using single-service towels. Note: If solution in dispenser becomes visibly dirty, replenish with fresh mixture of this product.

Contains:

Hydrogen Peroxide (from Sodium Percarbonate) = 17.0%

SAFE HANDLING WARNING

WARNING

KEEP OUT OF REACH OF CHILDREN

Causes serious eye damage

May intensify fire; oxidizer

Read label before use. Do not breathe dust or mist. Get medical advice and attention if you feel unwell. Store in a dry place. Store in a closed container.

FISRT AID:

IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.

IF ON SKIN: Wash with plenty of water.

IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing.

IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.

SEE SAFETY DATA SHEETS FOR MORE INFORMATION

KEEP OUT OF REACH OF CHILDREN

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

POD  CONCENTRATE
ultra-concentrated, premium, moderate-foam teat dip concentrate powder

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 76315-1009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Hydrogen Peroxide (UNII: BBX060AN9V) (Hydrogen Peroxide - UNII:BBX060AN9V)	Hydrogen Peroxide	17 kg  in 100 kg

Inactive Ingredients
Ingredient Name	Strength
Sodium Percarbonate (UNII: Z7G82NV92P)	56.5 kg  in 100 kg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76315-1009-1	45.4 kg in 1 DRUM
2	NDC: 76315-1009-2	181.6 kg in 1 DRUM

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/13/2013

Labeler - DeVere Company, Inc. (006074579)