Indications and uses
• For the temporary relief of symptoms including: • hay fever • congestion • stomach discomfort These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Histamine
- Manufacturer
- Deseret Biologials, Inc. | Apotheca Company
- Effective date
- 2024-03-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 5
- Source
- full-release
- Hydrated at
- 2026-06-01 02:26:23
Label at a glance#
ProductHistamine
Active ingredientHISTAMINE DIHYDROCHLORIDE
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.
Contacts and useful links#
Websitewww.desbio.com
www.desbio.com
www.desbio.comLabel contents#
Full prescribing information#
ACTIVE INGREDIENTS:
Histaminum Hydrochloricum 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.
PURPOSE:
Histaminum Hydrochloricum - Hay Fever, Congestion, Stomach Discomfort
USES:
• For the temporary relief of symptoms including:
• hay fever • congestion • stomach discomfort
These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
WARNINGS:
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.
Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.
KEEP OUT OF REACH OF CHILDREN:
In case of overdose, contact a physician or Poison Control Center right away.
DIRECTIONS:
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.
INACTIVE INGREDIENTS:
Demineralized water, 25% ethanol
QUESTIONS:
PACKAGE LABEL DISPLAY:
DesBio
Histamine
Homeopathic
NDC 43742-0696-1
1 FL OZ (30 ml)
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43742-0696-1 | Histamine | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 43742-0696 | HISTAMINE (HISTAMINUM HYDROCHLORICUM) LIQUID [DESERET BIOLOGIALS, INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20240316_f1503ad8-cb3b-4de5-a07c-57e5b80b756f.zip |
Products#
Every source-derived product name is available through these pages.
- Histamine
- Histaminum Hydrochloricum
- HISTAMINE DIHYDROCHLORIDE
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 43742-0696 | 43742-0696-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HISTAMINE DIHYDROCHLORIDE | 3POA0Q644U | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Histamine | HISTAMINUM HYDROCHLORICUM | Deseret Biologials, Inc. | f1503ad8-cb3b-4de5-a07c-57e5b80b756f | 2024-03-14 | Warnings | 43742-0696-1 43742-0696 43742069601 3a9ff815-750d-4247-970e-0620b5d44ddc f1503ad8-cb3b-4de5-a07c-57e5b80b756f |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.