Lactisan

Manufacturer: DeLaval | WestAgro, Inc. | WestAgro, Inc | K Klean dba WestAgro, Inc.
Effective date: 2021-12-16
Label type: OTC ANIMAL DRUG LABEL
Version: 6
Source: legacy-cache
Hydrated at: 2026-08-01 22:22:21

Label at a glance#

ProductLactisan

Active ingredientLACTIC ACID, L-, SORBITOL

Label structure13 sections

Storage and handling

STORAGE AND DISPOSAL THOROUGHLY RINSE ALL MEASURING DEVICES AND STORE OUT OF REACH OF CHILDREN. Store at room temperature. Avoid storing near heat or open flame. Do not store in direct sunlight. Avoid contact with food or feed. Keep container tightly closed when not in use. If product has frozen, thaw in a warm room and shake well before use. Do not reuse empty container. Rinse empty container before dispo...

Contacts and useful links#

PhoneLabel contact1-800-424-9300

PhoneLabel contact816-891-7700

Label contents#

Full prescribing information#

DeLaval Lactisan

INDICATIONS & USAGE SECTION

Concentrated Pre-Post Teat Sanitizer with Emollient

Aids in reducing the spread of mastitis-causing organisms

Sanitizante de pezones concentrado para antes y despues del ordeno. Contiene emolientes.

Ayuda a reducir la transmision de microorganismos que causan mastisis

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS:

Lactic Acid ................................ 14.0% w/w

Emollient* ................................ 20.0% w/w

After dilution according to directions:

Lactic Acid ................................ 3.5%

Emollient* ................................ 5.0%

* from Sorbitol

SPL UNCLASSIFIED SECTION

3000-C0116

NPE FREE Formula

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHLDREN

!CAUTION

MANTENER FUERA DEL ALCANCE DE LOS NINOS

!CUIDADO

SPL UNCLASSIFIED SECTION

3000

NDC 55756-000

GENERAL PRECAUTIONS SECTION

SI USTED NO PUEDE LEER ESTA ETIQUETA, POR FAVOR PIDA A ALGUIEN MAS QUE SE LA LEA ANTES DE USAR ESTE PRODUCTO

READ AND UNDERSTAND ALL INSTRUCTIONS BEFORE USING THIS PRODUCT

SPL UNCLASSIFIED SECTION

FIRST AID

Eye Contact: Flush with water. Remove contact lenses, if present, after first 5 minutes. Then continue rinsing. Get immediate medical attention.

If Swallowed: Do not induce vomiting. If victim is fully conscious, give large quantity of water. Never give anything my mouth to an unconscious person. Get immediate medical attention.

STORAGE AND HANDLING SECTION

STORAGE AND DISPOSAL

THOROUGHLY RINSE ALL MEASURING DEVICES AND STORE OUT OF REACH OF CHILDREN. Store at room temperature. Avoid storing near heat or open flame. Do not store in direct sunlight. Avoid contact with food or feed. Keep container tightly closed when not in use. If product has frozen, thaw in a warm room and shake well before use. Do not reuse empty container. Rinse empty container before disposing of in a safe manner. To discard teat dip, dilute with water and pour down drain.

SPL UNCLASSIFIED SECTION

CHEM-TREC EMERGENCY NUMBER 1-800-424-9300

SPL UNCLASSIFIED SECTION

Not for Human Use

Additional Information on Material Safety Data Sheet

INDICATIONS & USAGE SECTION

GENERAL INSTRUCTIONS

Lactisan is a premium, concentrated teat dip that dilutes to a 3.5% lactic acid pre and post dip.
DO NOT use Lactisan at full strength.
Consult your veterinarian before using a teat dip on a cow with sore or chapped teats.
Do not pour unused teat dip back into original container.
Do not use for cleaning or sanitizing equipment.
Thoroughly clean and sanitize teat dip cup before milking.
Dip solution should be changed if it becomes visibly dirty, or if sediment is introduced.
Discard any teat dip that becomes contaminated for any reason.
Good dairy practices suggest the thorough cleaning and sanitizing of teats before milking to avoid contamination and assist in the control of mastitis.


DILUTION / MIXING DIRECTIONS Add 1 gallon of Lactisan to 3 gallons of water and agitate until thoroughly mixed. Proper dilution of Lactisan will yield 3.5% lactic acid with 5% sorbitol for skin conditioning. Failure to follow these mixing instructions may cause injury to animals or reduce the effectiveness of the product as a teat dip.

PRE-DIPPING

Remove excess organic debris and forestrip. (If water is used, use a minimal amount and dry thoroughly with a clean, single-service paper towel before forestripping.)
Dip or spray cow's teats with properly diluted Lactisan teat dip.
Allow a 30 second contact time.
Dry teats thoroughly with a clean, single-service towel.
Attach milker unit.

POST-DIPPING

Immediately after milking unit is removed, dip or spray teats with diluted Lactisan.
Before exposing cows to below-freezing temperatures, the teats should be thoroughly dry to reduce the potential of frostbite. Failure to follow these instructions may result in frozen teats and injured animals.

SPL UNCLASSIFIED SECTION

Manufactured for: DeLaval, Inc.
11100 N. Congress Avenue
Kansas City, MO 64153
Phone: 816-891-7700
Manufactured by: WestAgro, Inc.
©2018, Made in USA

NET CONTENTS:

LOT NO.:

EXP. DATE:

US GAL ( LITERS)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
LACTIC ACID, L-	ACTIVE INGREDIENT	F9S9FFU82N	2
SORBITOL	ACTIVE INGREDIENT	506T60A25R	2
LACTIC ACID, L-	ACTIVE MOIETY	F9S9FFU82N	2
SORBITOL	ACTIVE MOIETY	506T60A25R	2
C9-11 PARETH-8	INACTIVE INGREDIENT	80E6PSE1XL	2
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	2
FD&C YELLOW NO. 5	INACTIVE INGREDIENT	I753WB2F1M	2
MAGNESIUM OXIDE	INACTIVE INGREDIENT	3A3U0GI71G	2
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	2
Water	INACTIVE INGREDIENT	059QF0KO0R	2
XANTHAN GUM	INACTIVE INGREDIENT	TTV12P4NEE	2

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

Lactisan
Lactic Acid
LACTIC ACID, L-
SORBITOL
Water
XANTHAN GUM
MAGNESIUM OXIDE
SODIUM LAURYL SULFATE
FD&C BLUE NO. 1
FD&C YELLOW NO. 5
C9-11 PARETH-8

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55756-000	55756-000-02, 55756-000-01, 55756-000-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
LACTIC ACID, L-	F9S9FFU82N	ACTIB
SORBITOL	506T60A25R	ACTIB
Water	059QF0KO0R	IACT
XANTHAN GUM	TTV12P4NEE	IACT
MAGNESIUM OXIDE	3A3U0GI71G	IACT
SODIUM LAURYL SULFATE	368GB5141J	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
C9-11 PARETH-8	80E6PSE1XL	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 3 · 139 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	CAPSULE, LIQUID FILLED / ORAL	0.08 mg		Exact identifier — unii candidate 37 equally ranked IID candidates
XANTHAN GUM	XANTHAN GUM	TTV12P4NEE	SOLUTION / OPHTHALMIC	0.6 %w/v		Exact identifier — unii candidate 29 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	PASTE, DENTIFRICE / DENTAL	NA		Exact identifier — unii candidate 37 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	TABLET / BUCCAL	0.11 mg		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	TABLET, SUGAR COATED / ORAL	NA		Exact identifier — unii candidate 37 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	OINTMENT / TOPICAL	0.01 %w/w		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	SYRUP / ORAL	0.05 mg/5ml		Exact identifier — unii candidate 37 equally ranked IID candidates
XANTHAN GUM	XANTHAN GUM	TTV12P4NEE	TROCHE / ORAL		948 mg	Exact identifier — unii candidate 29 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	LIQUID / ORAL	NA		Exact identifier — unii candidate 37 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	LOTION / TOPICAL	NA		Exact identifier — unii candidate 37 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	SYRUP / ORAL	0.1 mg		Exact identifier — unii candidate 22 equally ranked IID candidates
XANTHAN GUM	XANTHAN GUM	TTV12P4NEE	ENEMA / RECTAL		150 mg	Exact identifier — unii candidate 29 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	PASTE / DENTAL	NA		Exact identifier — unii candidate 37 equally ranked IID candidates
SODIUM LAURYL SULFATE	SODIUM LAURYL SULFATE	368GB5141J	TABLET, FOR SUSPENSION / ORAL		264 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	FILM / SUBLINGUAL	0.07 mg		Exact identifier — unii candidate 37 equally ranked IID candidates
SODIUM LAURYL SULFATE	SODIUM LAURYL SULFATE	368GB5141J	GEL / VAGINAL	0.2 %w/w		Exact identifier — unii candidate 42 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	POWDER / TOPICAL	NA		Exact identifier — unii candidate 22 equally ranked IID candidates
XANTHAN GUM	XANTHAN GUM	TTV12P4NEE	TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL		36 mg	Exact identifier — unii candidate 29 equally ranked IID candidates
SODIUM LAURYL SULFATE	SODIUM LAURYL SULFATE	368GB5141J	SPRAY / TOPICAL		7 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
XANTHAN GUM	XANTHAN GUM	TTV12P4NEE	SUSPENSION / ORAL		360 mg	Exact identifier — unii candidate 29 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	MOUTHWASH / BUCCAL	NA		Exact identifier — unii candidate 37 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	SUPPOSITORY / VAGINAL	NA		Exact identifier — unii candidate 22 equally ranked IID candidates
SODIUM LAURYL SULFATE	SODIUM LAURYL SULFATE	368GB5141J	SUSPENSION, EXTENDED RELEASE / ORAL	0.08 mg/1ml		Exact identifier — unii candidate 42 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	CONCENTRATE / BUCCAL	NA		Exact identifier — unii candidate 37 equally ranked IID candidates
XANTHAN GUM	XANTHAN GUM	TTV12P4NEE	GEL / TOPICAL		58 mg	Exact identifier — unii candidate 29 equally ranked IID candidates
XANTHAN GUM	XANTHAN GUM	TTV12P4NEE	SOLUTION / ORAL		84 mg	Exact identifier — unii candidate 29 equally ranked IID candidates
SODIUM LAURYL SULFATE	SODIUM LAURYL SULFATE	368GB5141J	SPONGE / TOPICAL	5 %w/w		Exact identifier — unii candidate 42 equally ranked IID candidates
SODIUM LAURYL SULFATE	SODIUM LAURYL SULFATE	368GB5141J	SUSPENSION / ORAL	705 mg		Exact identifier — unii candidate 42 equally ranked IID candidates
SODIUM LAURYL SULFATE	SODIUM LAURYL SULFATE	368GB5141J	TABLET, EFFERVESCENT / ORAL	1.5 mg		Exact identifier — unii candidate 42 equally ranked IID candidates
SODIUM LAURYL SULFATE	SODIUM LAURYL SULFATE	368GB5141J	CAPSULE / RESPIRATORY (INHALATION)	NA		Exact identifier — unii candidate 42 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	ELIXIR / ORAL	0.15 mg		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	CAPSULE, COATED, EXTENDED RELEASE / ORAL	NA		Exact identifier — unii candidate 37 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	CAPSULE, DELAYED RELEASE / ORAL		2 mg	Exact identifier — unii candidate 37 equally ranked IID candidates
XANTHAN GUM	XANTHAN GUM	TTV12P4NEE	LOZENGE / ORAL		1264 mg	Exact identifier — unii candidate 29 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	CAPSULE, EXTENDED RELEASE / ORAL		1 mg	Exact identifier — unii candidate 37 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	CAPSULE, DELAYED RELEASE PELLETS / ORAL	0.01 mg		Exact identifier — unii candidate 37 equally ranked IID candidates
XANTHAN GUM	XANTHAN GUM	TTV12P4NEE	GRANULE, FOR SUSPENSION / ORAL		450 mg	Exact identifier — unii candidate 29 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	TABLET, EXTENDED RELEASE / ORAL		4 mg	Exact identifier — unii candidate 37 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	TABLET, DELAYED RELEASE / ORAL	0.01 mg		Exact identifier — unii candidate 37 equally ranked IID candidates
SODIUM LAURYL SULFATE	SODIUM LAURYL SULFATE	368GB5141J	CAPSULE, EXTENDED RELEASE / ORAL		166 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
XANTHAN GUM	XANTHAN GUM	TTV12P4NEE	SUSPENSION / RECTAL		452 mg	Exact identifier — unii candidate 29 equally ranked IID candidates
MAGNESIUM OXIDE	MAGNESIUM OXIDE	3A3U0GI71G	CAPSULE, EXTENDED RELEASE / ORAL		75 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
SODIUM LAURYL SULFATE	SODIUM LAURYL SULFATE	368GB5141J	INSERT / VAGINAL		15 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
SODIUM LAURYL SULFATE	SODIUM LAURYL SULFATE	368GB5141J	TABLET / SUBLINGUAL	1.1 mg		Exact identifier — unii candidate 42 equally ranked IID candidates
SODIUM LAURYL SULFATE	SODIUM LAURYL SULFATE	368GB5141J	CAPSULE, DELAYED RELEASE / ORAL		46 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
SODIUM LAURYL SULFATE	SODIUM LAURYL SULFATE	368GB5141J	TABLET, CHEWABLE, EXTENDED RELEASE / ORAL		1 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
SODIUM LAURYL SULFATE	SODIUM LAURYL SULFATE	368GB5141J	TABLET, COATED / ORAL		123 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	CONCENTRATE / BUCCAL	NA		Exact identifier — unii candidate 22 equally ranked IID candidates
MAGNESIUM OXIDE	MAGNESIUM OXIDE	3A3U0GI71G	TABLET, FILM COATED / ORAL		80 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	SOLUTION / TOPICAL	0.06 %w/w		Exact identifier — unii candidate 22 equally ranked IID candidates
SODIUM LAURYL SULFATE	SODIUM LAURYL SULFATE	368GB5141J	GEL / TOPICAL	0.05 %w/w		Exact identifier — unii candidate 42 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	SOLUTION / DENTAL	NA		Exact identifier — unii candidate 37 equally ranked IID candidates
SODIUM LAURYL SULFATE	SODIUM LAURYL SULFATE	368GB5141J	OINTMENT / TOPICAL		14 mg	Exact identifier — unii candidate 42 equally ranked IID candidates
MAGNESIUM OXIDE	MAGNESIUM OXIDE	3A3U0GI71G	CAPSULE / ORAL		20 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	TABLET, CHEWABLE / ORAL	4.5 mg		Exact identifier — unii candidate 22 equally ranked IID candidates
FD&C BLUE NO. 1	FD&C BLUE NO. 1	H3R47K3TBD	FILM, SOLUBLE / ORAL	0.04 mg		Exact identifier — unii candidate 37 equally ranked IID candidates
XANTHAN GUM	XANTHAN GUM	TTV12P4NEE	TABLET, CHEWABLE, EXTENDED RELEASE / ORAL		6 mg	Exact identifier — unii candidate 29 equally ranked IID candidates
FD&C YELLOW NO. 5	FD&C YELLOW NO. 5	I753WB2F1M	TABLET, EXTENDED RELEASE / ORAL	2.03 mg		Exact identifier — unii candidate 22 equally ranked IID candidates
XANTHAN GUM	XANTHAN GUM	TTV12P4NEE	CREAM / TOPICAL		46 mg	Exact identifier — unii candidate 29 equally ranked IID candidates
XANTHAN GUM	XANTHAN GUM	TTV12P4NEE	TABLET / ORAL		56 mg	Exact identifier — unii candidate 29 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 · 5 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Join
SARCOLACTICUM ACIDUM	LACTIC ACID, L-	Boiron	dc019886-27cb-28f2-e053-2995a90a1be3	2026-04-27	Name fallback generic name: LACTIC ACID, L-
SARCOLACTICUM ACIDUM	LACTIC ACID, L-	Boiron	dca089a8-993b-263e-e053-2995a90aa730	2024-01-25	Name fallback generic name: LACTIC ACID, L-
SARCOLACTICUM ACIDUM	LACTIC ACID, L-	Boiron	dc65aa3f-c57a-1b6b-e053-2a95a90a3faa	2024-01-25	Name fallback generic name: LACTIC ACID, L-
SARCOLACTICUM ACIDUM	LACTIC ACID, L-	Boiron	dc77ea38-a71b-8d29-e053-2a95a90a14d4	2024-01-25	Name fallback generic name: LACTIC ACID, L-
SARCOLACTICUM ACIDUM	LACTIC ACID, L-	Borion	0c041754-793a-8aae-e063-6294a90ac248	2023-12-08	Name fallback generic name: LACTIC ACID, L-

Reported adverse events (FAERS/openFDA)#

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