LacticPlus

Manufacturer
PEKANA Naturheilmittel GmbH
Effective date
2022-12-21
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:19:03

Label at a glance#

ProductLacticPlus
Active ingredientLactic Acid, DL-
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ingredients:
Acidum sarcolacticum4X
Acidum sarcolacticum6X
Acidum sarcolacticum12X
Acidum sarcolacticum30X
Acidum sarcolacticum200X

INACTIVE INGREDIENT SECTION

Contains 19% alcohol by volume.

Indications

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

For relief of overly acidic stomach. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Dosage

DOSAGE & ADMINISTRATION SECTION

Unless otherwise prescribed, adults take 15-20 drops, 3 times per day. For pediatric dosages, consult your practitioner.

Warning

WARNINGS SECTION

OTC - ASK DOCTOR SECTION

If symptoms persist, contact a licensed practitioner. If you have known sensitivity to any of the ingredients, please consult your licensed practitioner before use. If you are pregnant or nursing a baby, seek the advice of a health care professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

STORAGE AND HANDLING SECTION

Protect from light and heat.

Tamper Evident

SPL UNCLASSIFIED SECTION

Do not use this product if tamper evident strip is broken or removed from base of cap.

OTC - QUESTIONS SECTION

To report adverse events, contact BioResource at 321B Blodgett Street, Cotati, CA 94931

SPL UNCLASSIFIED SECTION

Distributed by:
BioResource Inc.
Cotati, CA 94931

Manufactured by:
PEKANA®
GmbH
D-88353 Kisslegg

PRINCIPAL DISPLAY PANEL - 100 ml Bottle Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LacticPlus™
Oral Drops

Homeopathic Medicine

For relief of overly
acidic stomach

3.34 FL OZ
(100 ml)

PEKANA®

PRINCIPAL DISPLAY PANEL - 100 ml Bottle Box
PRINCIPAL DISPLAY PANEL - 100 ml Bottle Box

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59469-024-30LacticPlus100 mL in 1 BOTTLE, GLASSSOLUTION/ DROPS1005
59469-024-30LacticPlus1 in 1 BOXSOLUTION/ DROPS15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59469-024LACTICPLUS (LACTIC ACID, DL-) SOLUTION/ DROPS [PEKANA NATURHEILMITTEL GMBH]5Current NDC, Legacy NDC, 2 package rows20221223_0eac9953-bc7d-4bb3-b893-2c168cd198c0.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59469-02459469-024-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
Lactic Acid, DL-3B8D35Y7S4ACTIB
Water059QF0KO0RIACT
Alcohol3K9958V90MIACT

Source Document#

Source XML · Source PDF

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
LacticPlusLACTIC ACID, DL-PEKANA Naturheilmittel GmbH0eac9953-bc7d-4bb3-b893-2c168cd198c02022-12-21WarningsExact identifier
ndc (package): 59469-024-30
ndc (product): 59469-024
ndc11 (package): 59469002430
spl id: bd3d8481-1db1-4698-af9e-5c79e10bd34e
spl set id: 0eac9953-bc7d-4bb3-b893-2c168cd198c0

Reported adverse events (FAERS/openFDA)#

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