Prep-San Ultra

Manufacturer: Ecolab Inc.
Effective date: 2025-10-02
Label type: OTC ANIMAL DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 02:45:04

Label at a glance#

ProductPrep-San Ultra

Active ingredientLACTIC ACID, DODECYLBENZENESULFONIC ACID, SULFONATED OLEIC ACID

Label structure4 sections

Contacts and useful links#

PhoneLabel contact1 800 328 0026

PhoneLabel contact1 651 222 5352

PhoneLabel contact1 800 392 3392

Label contents#

Full prescribing information#

SAFE HANDLING WARNING SECTION

Danger

Causes severe skin burns and eye damage.

Wash skin thoroughly after handling. Wear protective gloves/ protective clothing/ eye protection/ face protection. Do not mix with bleach or other chlorinated products – will cause chlorine gas.

IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. IF ON SKIN (or hair): Remove/ Take off immediately all contaminated clothing. Rinse skin with water/ shower.

IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing. IF IN EYES: Rinse cautiously with water for several minutes. Remove

contact lenses, if present and easy to do. Continue rinsing. Immediately call a POISON CENTER or doctor/ physician. Wash contaminated clothing before reuse.

VETERINARY INDICATIONS SECTION

DIRECTIONS:

Consult your Ecolab representative for specific use instructions and recommended dispensing equipment.

PREP-SAN ULTRA MUST BE DILUTED BEFORE USE

DO NOT MIX WITH ANYTHING BUT COOL, POTABLE WATER

FOR USE ONLY IN A DISPENSING SYSTEM RECOMMENDED BY ECOLAB

Dilution Parameter: A dilute solution of a 0.5% lactic acid and 1.0% linear alkylate sulfonates teat dip will consist of 1 part Prep-San Ultra and 9 parts potable water by volume.

IMPORTANT: Do not mix Prep-San Ultra or diluted Prep-San Ultra with any other products unless specified in the product use instructions. If transferred from this container to any other, make sure that the other container is thoroughly pre-cleaned and bears the proper container labeling for Prep-San Ultra. If product in dip cup becomes visibly dirty, discard contents and replenish with diluted, ready-to-use product. Do not reuse or return any unused product to the original container.

Before Milking: Wash teats thoroughly just prior to next milking with appropriate udder wash solution or pre-milking teat dip to avoid contamination of milk. Teats should then be dried with single-service towels. Use proper procedures for udder washing or pre-dipping.

Application of Diluted Prep-San Ultra

Directions for Teat Dipping

Pre-Milk Dipping: Fill teat dip cup with diluted Prep-San Ultra. Before each cow is milked, dip each teat fulllength into the teat dip cup containing diluted Prep-San Ultra. Wipe teats dry after dipping using single-service towels to avoid contamination of milk.

Post-Milk Dipping: Immediately after each milking, dip each teat full-length into the teat dip cup containing diluted Prep-San Ultra. Allow to air dry. Do not wipe. Always use fresh, diluted Prep-San Ultra. Do not turn cows out in freezing weather until teat dip is completely dry.

Directions for Teat Spraying

Pre-Milk Spraying: Before each cow is milked, spray entire teat with diluted Prep-San Ultra. Wipe teats after spraying using single-service towels to avoid contamination of milk.

Post-Milk Spraying: Immediately after each milking, spray entire teat with diluted Prep-San Ultra. Allow to air dry. Do not wipe. Always use fresh, diluted Prep-San Ultra. Do not turn cows out in freezing weather until diluted Prep-San Ultra is completely dry.

Expanded Usage: When freshening cows, begin dipping teats twice daily for about 10 days before calving.

PRECAUTION: Prep-San Ultra is not intended to cure or help the healing of chapped or irritated teats. As with any germicide, irritation or sensitization may occur in sensitive animals. In case of teat irritation or chapping, have the condition examined and, if necessary, treated by a veterinarian.

NOTE: Use blended Prep-San Ultra within six (6) months of blended date.

OTHER SAFETY INFORMATION

READ SAFETY DATA SHEET (SDS) BEFORE USING THIS PRODUCT

EMERGENCY HEALTH INFORMATION: 1 800 328 0026. If located outside the United States and Canada, call collect
1 651 222 5352 (number is in the US).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

A & L Laboratories

Prep-San^™ Ultra

Teat Dip Concentrate

An aid in reducing the spread of organisms which may cause mastitis

ACTIVE INGREDIENTS:

Lactic acid................................................................................................4.2%

Linear alkylate sulfonates........................................................................8.2%

(includes 5.0% linear dodecyl benzene sulfonic acid and 3.2% sulfonated oleic acid)

INERT INGREDIENTS:................................................................................47.6%

SKIN CONDITIONING SYSTEM:

(contains sorbitol).................................................................................... 40.0%

TOTAL:.....................................................................................................100.0%

Manufactured by

Ecolab · 1 Ecolab Place · St. Paul, MN 55102 USA · tel: 1 800 392 3392

Made in U.S.A. | Hecho en EE.UU.

762092/5301/0517

56.8 L (15 US GAL) 6301638

representative label

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
LACTIC ACID, UNSPECIFIED FORM Pharmacologic Class Indexing	1	Indexing - Pharmacologic Class	20220121

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f52be47f-7aa7-46c0-b1fa-50c18dd50206	Product name	1	20201029
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
597b1cfd-7b31-5048-62be-ca5cd740da2f	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
47593-547-17	Prep-San Ultra	56800 mL in 1 DRUM	SOLUTION	56800	4
47593-547-21	Prep-San Ultra	208000 mL in 1 DRUM	SOLUTION	208000	4
47593-547-44	Prep-San Ultra	1150000 mL in 1 CONTAINER	SOLUTION	1150000	4

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
DODECYLBENZENESULFONIC ACID	ACTIVE INGREDIENT	60NSK897G9	1
LACTIC ACID	ACTIVE INGREDIENT	33X04XA5AT	1
DODECYLBENZENESULFONIC ACID	ACTIVE MOIETY	60NSK897G9	1
LACTIC ACID	ACTIVE MOIETY	33X04XA5AT	1
SORBITOL	INACTIVE INGREDIENT	506T60A25R	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Prep-San Ultra
Lactic acid, Linear dodecylbenzene sulfonic acid, Sulfonated oleic acid
LACTIC ACID
DODECYLBENZENESULFONIC ACID
SULFONATED OLEIC ACID
WATER
SORBITOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
47593-547	47593-547-17, 47593-547-21, 47593-547-44

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
Name	UNII	Kind
LACTIC ACID	33X04XA5AT	ACTIB
DODECYLBENZENESULFONIC ACID	60NSK897G9	ACTIB
SULFONATED OLEIC ACID	DDS68Y21OL	ACTIB
WATER	059QF0KO0R	IACT
SORBITOL	506T60A25R	IACT

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 · 44 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
SORBITOL	SORBITOL	506T60A25R	GUM, CHEWING / BUCCAL		5110 mg	Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	POWDER / ORAL		36000 mg	Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	EMULSION / TOPICAL	7 %w/w		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS	1.04 %w/v		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	LIQUID / TOPICAL	1 %w/w		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SOLUTION/ DROPS / OPHTHALMIC	0.25 %w/v		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	AEROSOL, FOAM / TOPICAL	4.95 %w/w		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	INJECTION / SUBCUTANEOUS	4.7 %w/v		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	INJECTION / INTRA-ARTICULAR	45 %w/v		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, ORALLY DISINTEGRATING / ORAL		7 mg	Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, COATED / ORAL	12.96 mg		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SYRUP / ORAL	4370 mg/5ml		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	INJECTION / INTRAVENOUS		1276 mg	Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	POWDER, FOR SUSPENSION / ORAL		12000 mg	Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	ELIXIR / ORAL	833.3 mg		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SUSPENSION / ORAL		45000 mg	Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	INJECTION / INTRASYNOVIAL	45 %w/v		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SOLUTION / OPHTHALMIC		6 mg	Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SUSPENSION / RECTAL	46.18 %w/v		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET / SUBLINGUAL	50.5 mg		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, DELAYED RELEASE / ORAL	0.01 mg		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	CREAM, AUGMENTED / TOPICAL	15 %w/w		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SOLUTION, CONCENTRATE / ORAL	300 mg/1ml		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SYSTEM / TOPICAL		6300 mg	Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	INJECTION, SOLUTION / SUBCUTANEOUS	4.7 %w/v		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	INJECTION, SOLUTION / INTRAVENOUS		4050 mg	Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	INJECTION / INTRAMUSCULAR	NA		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, CHEWABLE / ORAL		3555 mg	Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SOLUTION / NASAL	25 mg/1ml		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	CONCENTRATE / ORAL	600 mg/1ml		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	LOTION / TOPICAL	10.7 %w/w		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	CREAM / TOPICAL	36.8 %w/w		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, EXTENDED RELEASE / ORAL		428 mg	Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	PASTE, DENTIFRICE / DENTAL	14 %w/w		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SOLUTION / ORAL		29268 mg	Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	CAPSULE / ORAL		1111 mg	Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET / ORAL	337.28 mg		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	PASTE / DENTAL	14.6 %w/w		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	TABLET, FILM COATED / ORAL	5 mg		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	LIQUID / ORAL		53460 mg	Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	INJECTION / INTRALESIONAL	45 %w/v		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	OINTMENT / TOPICAL	10 %w/w		Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	SPRAY / NASAL		49 mg	Exact identifier — unii candidate 44 equally ranked IID candidates
SORBITOL	SORBITOL	506T60A25R	GUM, CHEWING / ORAL		6168 mg	Exact identifier — unii candidate 44 equally ranked IID candidates

Reported adverse events (FAERS/openFDA)#

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