EfferCept

Manufacturer
Activon | Longwood Scientific, LLC
Effective date
2022-12-19
Label type
OTC ANIMAL DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 02:41:48

Label at a glance#

ProductEfferCept
Active ingredientTROCLOSENE SODIUM
Label structure5 sections

Storage and handling

For Best Results Add tablets to any potable water and allow to fully dissolve before use. Use maximum strength during first 45 days of use, or if conditions are wet and muddy. For extra foaming of teat conditioning, add SoftGuard to solution. EfferCept solution may be used for up to 10 days. Use a clean container to store EfferCept solution. Keep tablets in a dry and tightly closed container between uses.

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

DILUTION RATES

PRE/POST TEAT DIP                  Tab/Gal.

Regular Strength                           2/1

Maximum Strength                        3/1

BULK DILUTION RATES

Gallons                  Regular Strength                  Maximum Strength

55 Gallons              220 Tablets (1 bag)              330 Tablets

275 Gallons          1100 Tablets (5 bags)           1650 Tablets

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT:

Sodium Dichloro-s-Triazinetrione................50%

INERT INGREDIENTS:.........................50%

Available Chlorine....30%   Total...............100%

STORAGE AND HANDLING SECTION

For Best Results

  • Add tablets to any potable water and allow to fully dissolve before use.
  • Use maximum strength during first 45 days of use, or if conditions are wet and muddy.
  • For extra foaming of teat conditioning, add SoftGuard to solution.
  • EfferCept solution may be used for up to 10 days.
  • Use a clean container to store EfferCept solution.
  • Keep tablets in a dry and tightly closed container between uses.

PRECAUTIONS SECTION

PRECAUTION: Keep out of reach of children. Do not take Internally. Not for human consumption. Do not mix with bleach, acids, ammonia, or non-ionic detergents.

EYE CONTACT: Flush eyes with clean water. Seek medical advice.

IF SWALLOWED: Drink large quantities of water, do not induce vomiting. Seek medical advice immediately.

DO NOT INHALE VAPORS from closed containers of stored solutions of EfferCept. Open in well ventilated areas.


PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FILL         ADD         USE

MAKES UP TO XX GAL

EfferCept

PRE/ POST TEAT DIP

Kills mastitis-causing organisms ON CONTACT

Use as a dip, spray, foam or scrub

Gentle on teats, skin, and udders

1540 TABLETS

(6 g/tablet)

Net WT. 20.37 lbs. (9.24 kg)

container labelcontainer label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1537585EfferCept 50 % Teat DipPSN7
1537580troclosene sodium 50 % Teat DipPSN7
1537585troclosene sodium 500 MG/ML Topical Solution [Effercept]SBD7
1537580troclosene sodium 500 MG/ML Topical SolutionSCD7
1537585EfferCept 50 % Topical SolutionSY7
1537585Effercept 500 MG/ML Topical SolutionSY7
1537580troclosene sodium 50 % Teat DipSY7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
14925-301-11EfferCept300 g in 1 BOXFOR SOLUTION3007
14925-301-12EfferCept1320 g in 1 BOXFOR SOLUTION13207
14925-301-13EfferCept9240 g in 1 BOXFOR SOLUTION92407

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
14925-301EFFERCEPT (TROCLOSENE SODIUM) FOR SOLUTION [ACTIVON]73 package rows20221220_b03c78fe-cc1d-43a3-bde4-bfd54f242cf4.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
14925-30114925-301-11, 14925-301-12, 14925-301-13

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
TROCLOSENE SODIUM07M9U9U0LKACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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