FDA.reportPublic FDA data

Stop-A-Leak

Manufacturer
H. W. Naylor Company Inc. | JOHNSON MATTHEY INC.
Effective date
2013-01-04
Label type
OTC ANIMAL DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:34:44

Label at a glance#

ProductStop-A-Leak
Active ingredientIodine
Label structure7 sections

Dosage and administration

With applicator attached to cap, apply Stop-A-Leak over opening in teat and over entire end of teat. Apply morning and night after milking until teat stops leaking. Strip quarter clean and thoroughly dry end of teat before applying Stop-A-Leak. In severe cases, milk out quarter and apply three times a day. Keep bottle tightly capped.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Iodine

Purpose

OTC - PURPOSE SECTION

for COW'S TEATS THAT LEAK MILK

Directions

DOSAGE & ADMINISTRATION SECTION

With applicator attached to cap, apply Stop-A-Leak over opening in teat and over entire end of teat. Apply morning and night after milking until teat stops leaking. Strip quarter clean and thoroughly dry end of teat before applying Stop-A-Leak. In severe cases, milk out quarter and apply three times a day. Keep bottle tightly capped.

Safety

GENERAL PRECAUTIONS SECTION

CAUTION

Treated teats should be thoroughly washed before milking. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into eyes or on mucous membranes

Other Ingredients

INACTIVE INGREDIENT SECTION

Tannic Acid, Ethyl Acetate. Ethylcellulose, lsopropyl Alcohol 22%.

Questions?

OTC - QUESTIONS SECTION

H. W. NAYLOR CO., INC.
MORRIS, N.Y. 13808 U.S.A.

Principal Display Panels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DIN - 297844

Dr. Naylor®

STOP-A-LEAK

for COWS' TEATS THAT LEAK MILK

Contains Iodine in a base of Tannic Acid, Ethyl Acetate, Ethylcellulose, Isopropyl Alcohol 22%.

1.75 Fluid Ozs.

H.W. NAYLOR CO., INC.
Morris N.Y. 13808 U.S.A.

Lot - XX-XX
Exp. MM-YY

Label
Label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
IodineACTIVE INGREDIENT9679TC07X42
IodineACTIVE MOIETY9679TC07X42
Ethyl AcetateINACTIVE INGREDIENT76845O8NMZ2
EthylcellulosesINACTIVE INGREDIENT7Z8S9VYZ4B2
Isopropyl AlcoholINACTIVE INGREDIENTND2M4163022
Tannic AcidINACTIVE INGREDIENT28F9E0DJY62

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
15878-21915878-219-11

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
Iodine9679TC07X4ACTIB
Tannic Acid28F9E0DJY6IACT
Ethyl Acetate76845O8NMZIACT
Ethylcelluloses7Z8S9VYZ4BIACT
Isopropyl AlcoholND2M416302IACT

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 · 30 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
EthylcellulosesETHYLCELLULOSE7Z8S9VYZ4BTABLET / ORAL300 mgExact identifier — unii candidate
14 equally ranked IID candidates
Isopropyl AlcoholISOPROPYL ALCOHOLND2M416302OIL / TOPICAL72 mgExact identifier — unii candidate
9 equally ranked IID candidates
Ethyl AcetateETHYL ACETATE76845O8NMZSYSTEM / TRANSDERMAL41 mgExact identifier — unii candidate
7 equally ranked IID candidates
Isopropyl AlcoholISOPROPYL ALCOHOLND2M416302LOTION, AUGMENTED / TOPICAL2070 mgExact identifier — unii candidate
9 equally ranked IID candidates
Isopropyl AlcoholISOPROPYL ALCOHOLND2M416302SWAB / TOPICAL43.9 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
EthylcellulosesETHYLCELLULOSE7Z8S9VYZ4BSYSTEM / TOPICAL10 mgExact identifier — unii candidate
14 equally ranked IID candidates
Ethyl AcetateETHYL ACETATE76845O8NMZSOLUTION / ORAL13 mgExact identifier — unii candidate
7 equally ranked IID candidates
Isopropyl AlcoholISOPROPYL ALCOHOLND2M416302SOLUTION / TOPICAL40 %w/vExact identifier — unii candidate
9 equally ranked IID candidates
EthylcellulosesETHYLCELLULOSE7Z8S9VYZ4BSUSPENSION, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
14 equally ranked IID candidates
Isopropyl AlcoholISOPROPYL ALCOHOLND2M416302GEL, METERED / TOPICAL525 mgExact identifier — unii candidate
9 equally ranked IID candidates
Ethyl AcetateETHYL ACETATE76845O8NMZTABLET, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
7 equally ranked IID candidates
Isopropyl AlcoholISOPROPYL ALCOHOLND2M416302TABLET, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
9 equally ranked IID candidates
Ethyl AcetateETHYL ACETATE76845O8NMZCAPSULE, EXTENDED RELEASE / ORAL382.26 mgExact identifier — unii candidate
7 equally ranked IID candidates
EthylcellulosesETHYLCELLULOSE7Z8S9VYZ4BTABLET, DELAYED RELEASE / ORAL53.8 mgExact identifier — unii candidate
14 equally ranked IID candidates
Isopropyl AlcoholISOPROPYL ALCOHOLND2M416302SPONGE / TOPICAL4 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
Ethyl AcetateETHYL ACETATE76845O8NMZSUSPENSION / ORALNAExact identifier — unii candidate
7 equally ranked IID candidates
EthylcellulosesETHYLCELLULOSE7Z8S9VYZ4BPOWDER / ORAL2090 mgExact identifier — unii candidate
14 equally ranked IID candidates
Isopropyl AlcoholISOPROPYL ALCOHOLND2M416302OIL / AURICULAR (OTIC)6 mgExact identifier — unii candidate
9 equally ranked IID candidates
EthylcellulosesETHYLCELLULOSE7Z8S9VYZ4BTABLET, FILM COATED / ORAL83 mgExact identifier — unii candidate
14 equally ranked IID candidates
Ethyl AcetateETHYL ACETATE76845O8NMZFILM, EXTENDED RELEASE / TRANSDERMAL0.05 mgExact identifier — unii candidate
7 equally ranked IID candidates
Ethyl AcetateETHYL ACETATE76845O8NMZSOLUTION / TOPICAL31 %w/wExact identifier — unii candidate
7 equally ranked IID candidates
EthylcellulosesETHYLCELLULOSE7Z8S9VYZ4BPOWDER, FOR SUSPENSION / ORALNAExact identifier — unii candidate
14 equally ranked IID candidates
EthylcellulosesETHYLCELLULOSE7Z8S9VYZ4BTABLET, FILM COATED, EXTENDED RELEASE / ORAL52.5 mgExact identifier — unii candidate
14 equally ranked IID candidates
Isopropyl AlcoholISOPROPYL ALCOHOLND2M416302GEL / TOPICAL75 mgExact identifier — unii candidate
9 equally ranked IID candidates
EthylcellulosesETHYLCELLULOSE7Z8S9VYZ4BTABLET, EXTENDED RELEASE / ORAL1120 mgExact identifier — unii candidate
14 equally ranked IID candidates
EthylcellulosesETHYLCELLULOSE7Z8S9VYZ4BTABLET, COATED / ORAL20 mgExact identifier — unii candidate
14 equally ranked IID candidates
EthylcellulosesETHYLCELLULOSE7Z8S9VYZ4BCAPSULE / ORAL12.32 mgExact identifier — unii candidate
14 equally ranked IID candidates
EthylcellulosesETHYLCELLULOSE7Z8S9VYZ4BCAPSULE, EXTENDED RELEASE / ORAL153 mgExact identifier — unii candidate
14 equally ranked IID candidates
EthylcellulosesETHYLCELLULOSE7Z8S9VYZ4BCREAM / TOPICALNAExact identifier — unii candidate
14 equally ranked IID candidates
EthylcellulosesETHYLCELLULOSE7Z8S9VYZ4BGRANULE, FOR SUSPENSION, EXTENDED RELEASE / ORAL1000 mgExact identifier — unii candidate
14 equally ranked IID candidates

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 · 11 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
IodineIODINENice-Pak Products, LLC857f13fe-51c9-4e5b-b5e2-a981dedabf712026-03-12Warnings, Adverse reactionsName fallback
generic name: IODINE
IodineIODINEUnited Natural Foods, Inc. dba UNFI8e840855-d210-4a99-b73f-6c69dcf2b6fb2026-02-16WarningsName fallback
generic name: IODINE
IODDO IODINEIODINEEVI LABS4af8552c-1f2b-84ad-e063-6394a90abb622026-02-16WarningsName fallback
generic name: IODINE
IodineIODINEWalgreen Co.d3d44c9f-4eb6-4e5b-9943-c0f80f06952d2026-02-12Warnings, Adverse reactionsName fallback
generic name: IODINE
IodiumIODINEBoiron85cd5e7a-52b6-0bb7-e053-2a91aa0aaa142023-11-13Name fallback
generic name: IODINE
IodiumIODINEBoiron85cd0c27-7859-5fd8-e053-2a91aa0a7c692023-11-13Name fallback
generic name: IODINE
IodiumIODINEBoiron85cd0c27-782d-5fd8-e053-2a91aa0a7c692023-11-13Name fallback
generic name: IODINE
IodiumIODINEBoiron724cb010-7c5d-11e6-8589-424c583030312023-11-13Name fallback
generic name: IODINE
IodiumIODINEBoiron85cd3f96-b800-f192-e053-2991aa0aee982023-02-20Name fallback
generic name: IODINE
IodiumIODINEBoiron85cd5e7a-52a7-0bb7-e053-2a91aa0aaa142023-01-23Name fallback
generic name: IODINE
IodiumIODINEBoiron85ccdc3f-5dd9-a5b1-e053-2a91aa0a8a0c2023-01-05Name fallback
generic name: IODINE

Reported adverse events (FAERS/openFDA)#

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