Antacid

Manufacturer
Liddell Laboratories, Inc. | Apotheca Company
Effective date
2022-04-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:02:58

Label at a glance#

ProductAntacid
Active ingredientSEMECARPUS ANACARDIUM JUICE, SILVER NITRATE, BISMUTH, MARSDENIA CONDURANGO BARK, GERANIUM MACULATUM ROOT, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, RANCID BEEF, ROBINIA PSEUDOACACIA BARK, SULFURIC ACID
Label structure9 sections

Dosage and administration

Adults and Children over 12: Spray twice under the tongue up to each 30 minutes until symptoms are relieved. As a preventative, spray twice under the tongue three times per day. Children 12 and under: Consult a doctor prior to use.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each spray) 10% of Anacardium Orientale 6X, Argentum Nitricum 6X, Bismuthum Metallicum 30C, Condurango 200C, Geranium Maculatum 3X, Nux Vomica 6X, Phosphorus 12X, Pyrogenium 30C, Robinia Pseudoacacia 6X, Sulphuricum Acidum 6X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms associated with heartburn & excess stomach acid: stomach pain, indigestion, nausea, bloating.**

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

WARNINGS:

WARNINGS SECTION

If symptoms persist, consult a doctor.

If pregnant or breast feeding, ask a doctor before use.

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

Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

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 call a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and Children over 12: Spray twice under the tongue up to each 30 minutes until symptoms are relieved. As a preventative, spray twice under the tongue three times per day.

Children 12 and under: Consult a doctor prior to use.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Organic alcohol 20% v/v, Purified water.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms associated with heartburn & excess stomach acid: stomach pain, indigestion, nausea, bloating.**

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

QUESTIONS:

OTC - QUESTIONS SECTION

DIST. BY LIDDELL LABORATORIES, INC.

WOODBINE, IA 51579

WWW.LIDDELL.NET 1-800-460-7733

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ORAL SPRAYS

LIDDELL

LABORATORIES

EST. 1994

12A-a

Antacid

HOMEOPATHIC

1.0 FL. OZ. (30 ml)

AntacidAntacid

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50845-0256-12022-04-20C16284748780-1ba0f9c33-508d-a910-e053-dadaa90a0b85Drug Facts:
50845-0256-12021-01-29C16284748780-1ba0f9c33-508d-a910-e053-dadaa90a0b85Drug Facts:

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50845-025650845-0256-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

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
872d0f39-ccb3-4395-b1cd-1658d673c99fe3b56054-975a-4cd7-aa9b-86f270635fbf2022-04-20WarningsExact identifier
spl id: 872d0f39-ccb3-4395-b1cd-1658d673c99f
spl set id: e3b56054-975a-4cd7-aa9b-86f270635fbf

Reported adverse events (FAERS/openFDA)#

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