Reflux

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2021-06-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:14:36

Label at a glance#

ProductReflux
Active ingredientADENOSINE TRIPHOSPHATE DISODIUM, NADIDE, SILVER NITRATE, IPECAC, ROBINIA PSEUDOACACIA BARK, SULFUR, OREGANO, SUS SCROFA DUODENUM, SUS SCROFA ESOPHAGUS, SUS SCROFA UMBILICAL CORD, SUS SCROFA STOMACH, STRYCHNOS NUX-VOMICA SEED, COUMARIN, CENTAURIUM ERYTHRAEA, PANCRELIPASE, HYDROCHLORIC ACID, ANHYDROUS CITRIC ACID, FORMIC ACID, LACTIC ACID, L-, COENZYME A, PROTEUS MORGANII
Label structure9 sections

Dosage and administration

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Adenosinum Triphosphoricum Dinatrum 6X, 8X, Nadidum 6X, 8X, Argentum Nitricum 6X, 10X, Ipecacuanha 6X, 10X, Robinia Pseudoacacia 6X, 10X, Sulphur 6X, 10X, Origanum Vulgare 6X, 10X, 30X, Duodenum (Suis) 8X, Esophagus (Suis) 8X, Funiculus Umbilicalis Suis 8X, Stomach (Suis) 8X, Nux Vomica 8X, 10X, 30X, Coumarinum 8X, 10X, 30X, 200X, Erythraea Centaurium 10X, 30X, Pancreatinum 12X, Muriaticum Acidum 6C, 12C, 30C, 200C, Citricum Acidum 6C, 30C, 200C, Formicum Acidum 6C, 30C, 200C, Sarcolacticum Acidum 6C, 30C, 200C, Coenzyme A 8C, 10C, Proteus (Morgani) 30C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of symptoms related to heartburn and esophageal reflux.**

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

WARNINGS:

WARNINGS SECTION

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

If pregnant or breast-feeding, ask a health professional before use.

Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of symptoms related to heartburn and esophageal reflux.**

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.
469 W. Parkland Drive
Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 43742-1630-1

HOMEOPATHIC

REFLUX

1 FL OZ (30 ml)

RefluxReflux

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0b1603b8-969e-b082-f6f5-ad66d8a6ea8aProduct name220200325
19041f15-771b-3d3a-88fc-f5e2d079cd6dProduct name220200325
1987d950-08e4-4b70-adeb-fb67a71142abProduct name220200325
8825ddf7-1520-4680-b0ee-684e2fa73672Product name220200325
267a6f34-90b4-2f48-3063-4f505d06a7beProduct name120140508
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-1630REFLUX (ADENOSINUM TRIPHOSPHORICUM DINATRUM, NADIDUM, ARGENTUM NITRICUM, IPECACUANHA, ROBINIA PSEUDOACACIA, SULPHUR, ORIGANUM VULGARE, DUODENUM (SUIS), ESOPHAGUS (SUIS), FUNICULUS UMBILICALIS SUIS, STOMACH (SUIS), NUX VOMICA, COUMARINUM, ERYTHRAEA CENTAURIUM, PANCREATINUM, MURIATICUM ACIDUM, CITRICUM ACIDUM, FORMICUM ACIDUM, SARCOLACTICUM ACIDUM, COENZYME A, PROTEUS (MORGANI)) LIQUID [DESERET BIOLOGICALS, INC.]2Legacy NDC20210629_4c0ed459-4abd-4ebe-810a-8f92ff1986f8.zip

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-163043742-1630-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 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
2d947b58-2f33-44d8-97cb-a4d5ae0b7db24c0ed459-4abd-4ebe-810a-8f92ff1986f82021-06-28WarningsExact identifier
spl id: 2d947b58-2f33-44d8-97cb-a4d5ae0b7db2
spl set id: 4c0ed459-4abd-4ebe-810a-8f92ff1986f8

Reported adverse events (FAERS/openFDA)#

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