DIARALIA
- Manufacturer
- BOIRON | BOIRON, INC.
- Effective date
- 2023-05-10
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 6
- Source
- full-release
- Hydrated at
- 2026-06-01 02:21:09
Label at a glance#
ProductDIARALIA
Active ingredientPODOPHYLLUM, CINCHONA OFFICINALIS BARK, ARSENIC TRIOXIDE
Label structure12 sections
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredients** (in each tablet)
Arsenicum album 9C HPUS (0.83 mg)
Cinchona officinalis 5C HPUS (0.83 mg)
Podophyllum peltatum 9C HPUS (0.83 mg)
The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.
INDICATIONS & USAGE SECTION
Uses*
temporarily relieves symptoms of diarrhea such as:
- traveler's diarrhea
- intestinal pain
- bloating
- gas
- nausea
- vomiting
OTC - PURPOSE SECTION
Purpose*
Arsenicum album 9C HPUS (0.83 mg) ... Relieves diarrhea with nausea, vomiting, and weakness. (contains less that 10 -18 mg arsenic)
Cinchona officinalis 5C HPUS (0.83 mg) ... Relieves diarrhea with gas and bloating
Podophyllum peltatum 9C HPUS (0.83 mg) ... Relieves diarrhea with intestinal rumbling and pain
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have
fever
bloody or black stool
mucus in your stool.
OTC - STOP USE SECTION
Stop use and ask a doctor if symptoms persist for more than 2 days or worsen.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Drink plenty of clear fluids to help prevent dehydration caused by diarrhea.
- Adults and children 6 years of age and older: At the onset of symptoms, dissolve 2 tablets in the mouth every 4 to 6 hours, up to 2 days maximum. Discontinue use as soon as symptoms disappear.
- Children under 6 years of age: Ask a doctor.
SPL UNCLASSIFIED SECTION
do not use if glued carton end flaps are open or if the blister seal is broken.
store below 86° F (30° C)
60 Meltaway Tablets
No Known Drug Interactions
Diarrhea Relief*
Intestinal Pain Nausea Traveler's Diarrhea*
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
*C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.
INACTIVE INGREDIENT SECTION
lactose, croscarmellose sodium, magnesium stearate
OTC - QUESTIONS SECTION
1-800-BOIRON-1 (1-800-264-7661),
BoironUSA.com Info@boiron.com
Distributed by Boiron, Inc. Newtown Square, PA 19073
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 63f39a63-5cd1-4016-bd86-2bbb0f6c3139 | Product name | 3 | 20240506 |
| e5a77e9c-c528-733a-173d-914a234c024b | Product name | 5 | 20240506 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0220-9095-04 | 2023-04-12 | C162847 | 48780-1 | f386c64a-06df-0266-e053-dadaa90a7c1a | DIARALIA |
| 0220-9095-04 | 2023-01-30 | C162847 | 48780-1 | f386c64a-06df-0266-e053-dadaa90a7c1a | DIARALIA |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0220-9095-04 | DIARALIA | 60 in 1 CARTON | TABLET | 60 | 6 | |
| 0220-9095-04 | DIARALIA | 60 in 1 BLISTER PACK | TABLET | 60 | 6 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- DIARALIA
- ARSENIC TRIOXIDE,CINCHONA OFFICINALIS BARK, PODOPHYLLUM
- CROSCARMELLOSE SODIUM
- CROSCARMELLOSE
- PODOPHYLLUM
- CINCHONA OFFICINALIS BARK
- MAGNESIUM STEARATE
- ARSENIC TRIOXIDE
- ARSENIC CATION (3+)
- LACTOSE, UNSPECIFIED FORM
- ANHYDROUS LACTOSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0220-9095 | 0220-9095-04 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CROSCARMELLOSE SODIUM | M28OL1HH48 | IACT |
| PODOPHYLLUM | 2S713A4VP3 | ACTIB |
| CINCHONA OFFICINALIS BARK | S003A158SB | ACTIB |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| ARSENIC TRIOXIDE | S7V92P67HO | ACTIB |
| LACTOSE, UNSPECIFIED FORM | J2B2A4N98G | 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 |
|---|---|---|---|---|---|---|
| DIARALIA | ARSENIC TRIOXIDE,CINCHONA OFFICINALIS BARK, PODOPHYLLUM | BOIRON | 8f665d4b-2d9b-8b5a-e053-2995a90a4caa | 2023-05-10 | 0220-9095-04 0220-9095 00220909504 fb5a86ae-243a-f9a0-e053-6394a90a504b 8f665d4b-2d9b-8b5a-e053-2995a90a4caa |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.