Lactistat

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-28
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:28:32

Label at a glance#

ProductLactistat
Active ingredientARSENIC TRIOXIDE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, ANAMIRTA COCCULUS SEED, GRAPHITE, HYDROFLUORIC ACID, LACHESIS MUTA VENOM, LACTIC ACID, DL-, TOXICODENDRON PUBESCENS LEAF, RUTA GRAVEOLENS FLOWERING TOP, LACTIC ACID, L-, SUCROSE
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 9.09% Arsenicum Album 12X, Calcarea Carbonica 12X, Cocculus Indicus 12X, Graphites 12X, Hydrofluoricum Acidum 12X, Lachesis Mutus 12X, Lacticum Acidum 12X, Rhus Tox 12X, Ruta Graveolens 12X, Sarcolacticum Acidum 12X, Saccharum Officinale 30X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms associated with lactic acid such as muscle weakness, muscle cramps and stiffness, and burning pain.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

If pregnant or breastfeeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing.

Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms associated with lactic acid such as muscle weakness, muscle cramps and stiffness, and burning pain.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.
201 Apple Blvd.
Woodbine, IA 51579    800.868.8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

LACTISTAT

1 fl. oz. (30 ml)

LactistatLactistat

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0336-12024-10-28C16284748780-1ba0f9c33-272b-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0336-12023-01-30C16284748780-1ba0f9c33-272b-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0336-12021-10-28C16284748780-1ba0f9c33-272b-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0336-12021-01-29C16284748780-1ba0f9c33-272b-a910-e053-dadaa90a0b85DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0336-1Lactistat30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0336LACTISTAT (ARSENICUM ALBUM, CALCAREA CARBONICA, COCCULUS INDICUS, GRAPHITES, HYDROFLUORICUM ACIDUM, LACHESIS MUTUS, LACTICUM ACIDUM, RHUS TOX, RUTA GRAVEOLENS, SARCOLACTICUM ACIDUM, SACCHARUM OFFICINALE) LIQUID [ENERGIQUE, INC.]4Current NDC, Legacy NDC, 1 package rows20241030_8dcc4a3a-9f21-4a77-ae42-b2c8283a076a.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-033644911-0336-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LactistatARSENICUM ALBUM, CALCAREA CARBONICA, COCCULUS INDICUS, GRAPHITES, HYDROFLUORICUM ACIDUM, LACHESIS MUTUS, LACTICUM ACIDUM, RHUS TOX, RUTA GRAVEOLENS, SARCOLACTICUM ACIDUM, SACCHARUM OFFICINALEEnergique, Inc.8dcc4a3a-9f21-4a77-ae42-b2c8283a076a2024-10-28WarningsExact identifier
ndc (package): 44911-0336-1
ndc (product): 44911-0336
ndc11 (package): 44911033601
spl id: 49acc937-c24f-4f2a-b72c-e3457e0844e1
spl set id: 8dcc4a3a-9f21-4a77-ae42-b2c8283a076a

Reported adverse events (FAERS/openFDA)#

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