FDA.reportPublic FDA data

Acetaldehyde

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2017-03-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:17:57

Label at a glance#

ProductAcetaldehyde
Active ingredientACETALDEHYDE
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

Acetaldehyde 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of symptoms caused by sensitivities to perfumes, flavors, dyes, plastics, alcohol or foods including sneezing, headache, bronchitis, difficult breathing, and digestive malfunction.**

**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, seek advice of 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 caused by sensitivities to perfumes, flavors, dyes, plastics, alcohol or foods including sneezing, headache, bronchitis, difficult breathing, and digestive malfunction.**

**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 43742-0712-1

HOMEOPATHIC

ACETALDEHYDE

1 FL OZ (30 ml)

AcetaldehydeAcetaldehyde

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-071243742-0712-1

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
ACETALDEHYDEGO1N1ZPR3BACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
3da76a0c-c1bf-4bc4-9f97-2c0271f71980cb26ed4d-8ebd-4b29-bf16-419d9278a7ef2017-03-02WarningsExact identifier
spl id: 3da76a0c-c1bf-4bc4-9f97-2c0271f71980
spl set id: cb26ed4d-8ebd-4b29-bf16-419d9278a7ef

Reported adverse events (FAERS/openFDA)#

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