DOSAGE & ADMINISTRATION SECTION
How to Use
Take with water 3-4 times a day. Ages 12 or older, 5 Pellets, Ages 12-2, 3 Pellets, Ages below 2, consult your Doctor.
Bestmade Natural Products Nat Sulph
- Manufacturer
- Bestmade Natural Products | Total Operations Management LLC DBA: Bestmade Natural Products Micro
- Effective date
- 2025-03-21
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 02:32:44
Label at a glance#
ProductBestmade Natural Products Nat Sulph
Active ingredientSODIUM SULFATE
Label structure8 sections
Label contents#
Full prescribing information#
INACTIVE INGREDIENT SECTION
Ingredients
Inactive: Lactose Pellet Base to Preserve Product
INDICATIONS & USAGE SECTION
Uses
Temporarily relieves discomfort due to musculoskeletal issues, occasional aches or pressure in the chest, water retention, irregular body secretions, congestion, greenish sputum, joint aches, and more. Temporarily supports fluid balance.*
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
This product is not intended to diagnose, treat, cure, or prevent any disease.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: Natrum Sulphuricum (Sodium Sulphate) 6x potency
OTC - PURPOSE SECTION
Uses
Temporarily relieves discomfort due to musculoskeletal issues, occasional aches or pressure in the chest, water retention, irregular body secretions, congestion, greenish sputum, joint aches, and more. Temporarily supports fluid balance.*
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
This product is not intended to diagnose, treat, cure, or prevent any disease.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Warnings and Storage:
Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms. Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place.
WARNINGS SECTION
Warnings and Storage:
Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms. Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place.
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
This product is not intended to diagnose, treat, cure, or prevent any disease.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Entire package label
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82969-1011-1 | Bestmade Natural Products Nat Sulph | 6 [hp_X] in 1 BOTTLE, GLASS | TABLET, SOLUBLE | 6 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 82969-1011 | BESTMADE NATURAL PRODUCTS NAT SULPH (NAT SULPH) TABLET, SOLUBLE [BESTMADE NATURAL PRODUCTS] | 4 | Current NDC, Legacy NDC, 1 package rows | 20250323_e9ea2ea5-d1f2-6678-e053-2a95a90a278f.zip |
Products#
Every source-derived product name is available through these pages.
- Bestmade Natural Products Nat Sulph
- Nat Sulph
- SODIUM SULFATE
- SODIUM CATION
- LACTOSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 82969-1011 | 82969-1011-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM SULFATE | 0YPR65R21J | ACTIB |
| LACTOSE | 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 |
|---|---|---|---|---|---|---|
| Bestmade Natural Products Nat Sulph | NAT SULPH | Bestmade Natural Products | e9ea2ea5-d1f2-6678-e053-2a95a90a278f | 2025-03-21 | Warnings | 82969-1011-1 82969-1011 82969101101 30d8c967-3cee-e336-e063-6294a90a6f07 e9ea2ea5-d1f2-6678-e053-2a95a90a278f |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.