FDA.reportPublic FDA data

FROST-PROOF

Manufacturer
Dairy Dynamics L.L.C.
Effective date
2015-01-13
Label type
OTC ANIMAL DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:39:52

Label at a glance#

ProductFROST-PROOF
Active ingredientCHLORHEXIDINE DIACETATE
Label structure14 sections

Label contents#

Full prescribing information#

WARNINGS AND PRECAUTIONS SECTION

Dairy Dynamics

INDUSTRIAL STRENGTH FORMULATIONS FOR THE COMMERCIAL DAIRY

AMERICAN OWNED AND OPERATED

WARNINGS AND PRECAUTIONS SECTION

PRECAUTIONARY STATEMENTS

Cause Eye Irritation.

May Be Harmful if Swallowed.

Avoid Inhalation.

SPL UNCLASSIFIED SECTION

FIRST AID

EYES:  Flush with large volumes of cold water for at least 15 minutes.

Internal:  If swallowed, Rinse mouth then give small amount/glass of water.

Get medical attention immediately.  Never give anything by mouth to an unconscious person.

Inhalation:  Avoid inhalation.  If respiratory difficulty develops remove victim to fresh air.  If difficulty persists give oxygen or artificial respiration.

Seek medical attention.

SPL UNCLASSIFIED SECTION

For Hazardous Materials (or dangerous goods) Incidents ONLY (spill, leak, fire, exposure or accident) Call CHEMTREC at 800-424-9300

SPL UNCLASSIFIED SECTION

Read Material Safety Data Sheet (MSDS) Before Using This Product!

INSTRUCTIONS FOR USE SECTION

DIRECTIONS FOR USE

POST DIPPING:  Immediately after milking, dip or dust teats with Frost-Proof powdered teat dip.  Ensure coverage of entire teat.

If this product becomes dirty, moist or hardens, discard contents of teat cup and refill with fresh material.

Use product as is.  Do not dilute.  Never return product to this container. 

Store in dry area.

OTC - ACTIVE INGREDIENT SECTION

Frost-Proof

Active ingredient:  Chlorhexidene DiAcetate   .5%

INACTIVE INGREDIENT SECTION

Contains Aloe-Vera for skin conditining.

OTC - PURPOSE SECTION

Usage:  For post milking teat dipping dairy cows.

SPL UNCLASSIFIED SECTION

TAKE TIME OBSERVE LABEL DIRECTIONS

SPL UNCLASSIFIED SECTION

NET CONTENTS:  15 US Lbs

SPL UNCLASSIFIED SECTION

Manufactured by:  Dairy Dynamics  17820 Washington St  Union, IL 60180

SPL UNCLASSIFIED SECTION

TDX-80P-DDC

LOT:

Exp:

03.03

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CHLORHEXIDINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
bb6d6c68-649d-4e6d-a1f6-603d969c8f68Product name120160303

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67351-980-04FROST-PROOF2.27 kg in 1 PAILPOWDER2.271
67351-980-14FROST-PROOF6.8 kg in 1 PAILPOWDER6.81
67351-980-25FROST-PROOF113.4 kg in 1 DRUMPOWDER113.41
67351-980-29FROST-PROOF13.61 kg in 1 PAILPOWDER13.611
67351-980-60FROST-PROOF27.22 kg in 1 DRUMPOWDER27.221

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67351-980FROST-PROOF (CHLORHEXIDINE DIACETATE) POWDER [DAIRY DYNAMICS L.L.C.]15 package rows20150115_cfe25c40-e023-4ef7-9752-382e65cc290b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CHLORHEXIDINE DIACETATEACTIVE INGREDIENT5908ZUF22Y1
CHLORHEXIDINEACTIVE MOIETYR4KO0DY52L1
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0X1
ALUMINUM SILICATEINACTIVE INGREDIENTT1FAD4SS2M1
AMMONIUM CHLORIDEINACTIVE INGREDIENT01Q9PC255D1
DIDECYLDIMONIUM CHLORIDEINACTIVE INGREDIENTJXN40O9Y9B1

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
67351-98067351-980-04, 67351-980-14, 67351-980-29, 67351-980-60, 67351-980-25

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
CHLORHEXIDINE DIACETATE5908ZUF22YACTIM
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
ALUMINUM SILICATET1FAD4SS2MIACT
AMMONIUM CHLORIDE01Q9PC255DIACT
ALOE VERA LEAFZY81Z83H0XIACT

Source Document#

Source XML · Source PDF

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 · 9 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALUMINUM SILICATEALUMINUM SILICATET1FAD4SS2MSYSTEM / TOPICAL19 mgExact identifier — unii candidate
4 equally ranked IID candidates
AMMONIUM CHLORIDEAMMONIUM CHLORIDE01Q9PC255DTABLET, FILM COATED / ORAL8 mgExact identifier — unii candidate
5 equally ranked IID candidates
AMMONIUM CHLORIDEAMMONIUM CHLORIDE01Q9PC255DTABLET, EXTENDED RELEASE / ORAL21 mgExact identifier — unii candidate
5 equally ranked IID candidates
ALUMINUM SILICATEALUMINUM SILICATET1FAD4SS2MTABLET, COATED / ORAL50 mgExact identifier — unii candidate
4 equally ranked IID candidates
AMMONIUM CHLORIDEAMMONIUM CHLORIDE01Q9PC255DSYRUP / ORAL131.68 mg/5mlExact identifier — unii candidate
5 equally ranked IID candidates
AMMONIUM CHLORIDEAMMONIUM CHLORIDE01Q9PC255DTABLET / ORAL8 mgExact identifier — unii candidate
5 equally ranked IID candidates
AMMONIUM CHLORIDEAMMONIUM CHLORIDE01Q9PC255DCAPSULE / ORAL8 mgExact identifier — unii candidate
5 equally ranked IID candidates
ALUMINUM SILICATEALUMINUM SILICATET1FAD4SS2MTABLET, EXTENDED RELEASE / ORAL94 mgExact identifier — unii candidate
4 equally ranked IID candidates
ALUMINUM SILICATEALUMINUM SILICATET1FAD4SS2MTABLET / ORAL19.25 mgExact identifier — unii candidate
4 equally ranked IID candidates

Reported adverse events (FAERS/openFDA)#

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