Active Ingredient
Hydraetis canadensis 6X
Kali muriaticum 3X
Pulsatilla 6X
Sanguinaria canadensis 6X
Silcea 6X
ALPHA SH
- Manufacturer
- Schwabe Mexico, S.A. de C.V.
- Effective date
- 2022-03-22
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 02:17:12
Label at a glance#
ProductALPHA SH
Active ingredientSANGUINARIA CANADENSIS ROOT, GOLDENSEAL, SILICON DIOXIDE, POTASSIUM CHLORIDE, PULSATILLA VULGARIS
Label structure11 sections
Label contents#
Full prescribing information#
INACTIVE INGREDIENT
Cellulose
Lactose monohydrate
Magnesium stearate
Purpose
Temporarily relieves these symptoms: helps decongest sinus openings and passages, shrinks swollen nasal membranes and promotes sinus drainage.
Indications & Usage
Temporarily relieves these symptoms: helps decongest sinus openings and sinus passages, shrinks swollen nasal membranse, promotes sinus drainage.
Dosage & Administration
Directions:
Sublingual medication. Place tablets under tongue at least 15 minutes before or 30m minutes after eating, brushing teeth, or drinking anything except water.
Adults and children 12 years of age and older: Take 2 tablets every 2 hours until relieved.
Children 2 to 12: Take 1 every 2 hours until relieved
Children under 2: Consult a physician.
Warnings
Do not use this product for headache pain for more than 10 days (for adults) or 5 days (for children).
Stop use
Stop use and ask a doctor if symptoms persist, get worse, or are accompanied by a high fever, or if new symptoms occur.
These can be signs of a serious condition.
Pregnancy or Breast Feeding
If pregnant or breast feeding, ask a healthcare professional before use.
Keep out of reach of children
Keep out of reach of children
Overdose
In case of overdose, seek medical help or contact a Poison Control Center immediately.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68466-4191-1 | ALPHA SH | 10 in 1 BLISTER PACK | TABLET | 10 | 3 | |
| 68466-4191-1 | ALPHA SH | 4 in 1 BOX | TABLET | 4 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68466-4191 | ALPHA SH (SANGUINARIA CANADENSIS ROOT, GOLDENSEAL, SILICON DIOXIDE, POTASSIUM CHLORIDE, PULSATILLA VULGARIS ) TABLET [SCHWABE MEXICO, S.A. DE C.V.] | 3 | Current NDC, Legacy NDC, 2 package rows | 20220323_3e2e5f52-db54-4635-83a8-a67a683c093c.zip |
Products#
Every source-derived product name is available through these pages.
- ALPHA SH
- SANGUINARIA CANADENSIS ROOT, GOLDENSEAL, SILICON DIOXIDE, POTASSIUM CHLORIDE, PULSATILLA VULGARIS
- SANGUINARIA CANADENSIS ROOT
- GOLDENSEAL
- SILICON DIOXIDE
- POTASSIUM CHLORIDE
- POTASSIUM CATION
- PULSATILLA VULGARIS
- LACTOSE MONOHYDRATE
- MAGNESIUM STEARATE
- CELLULOSE, MICROCRYSTALLINE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 68466-4191 | 68466-4191-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SANGUINARIA CANADENSIS ROOT | N9288CD508 | ACTIB |
| GOLDENSEAL | ZW3Z11D0JV | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | ACTIB |
| POTASSIUM CHLORIDE | 660YQ98I10 | ACTIB |
| PULSATILLA VULGARIS | I76KB35JEV | ACTIB |
| LACTOSE MONOHYDRATE | EWQ57Q8I5X | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| CELLULOSE, MICROCRYSTALLINE | OP1R32D61U | 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 |
|---|---|---|---|---|---|---|
| ALPHA SH | SANGUINARIA CANADENSIS ROOT, GOLDENSEAL, SILICON DIOXIDE, POTASSIUM CHLORIDE, PULSATILLA VULGARIS | Schwabe Mexico, S.A. de C.V. | 3e2e5f52-db54-4635-83a8-a67a683c093c | 2022-03-22 | Warnings | 68466-4191-1 68466-4191 68466419101 32449721-13e2-4194-b1c1-8e1dc3b33de4 3e2e5f52-db54-4635-83a8-a67a683c093c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.