warnings
WARNINGS: IF PREGNANT OR BREAST - FEEDING, ask a health professional before use. If symptoms worsen or persist for more than a week, discontinue use and contact a doctor. KEEP OUT OF THE REACH OF CHILDREN.
Weight Control
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Weight Control
- Generic name
- ACETICUM AC, ANACARD OR, BARYTA IOD, CALC CARB, CAPSICUM, FUCUS, GRAPHITES,, NAT SULPHURICUM, PHYTOLACCA, STANNUM MET, THYROIDINUM, ZINC MET.
- Manufacturer
- OHM PHARMA INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 32b7b539-ee54-4c80-a6d9-c159600927f5
- SPL ID
- d44beeee-4d22-68c3-e053-2a95a90a79ec
- Version
- 6
- Effective date
- 2021-12-29
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:19:35
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Weight Control | openfda.brand_name | |
| generic name | ACETICUM AC, ANACARD OR, BARYTA IOD, CALC CARB, CAPSICUM, FUCUS, GRAPHITES,, NAT SULPHURICUM, PHYTOLACCA, STANNUM MET, THYROIDINUM, ZINC MET. | openfda.generic_name | |
| manufacturer name | OHM PHARMA INC. | openfda.manufacturer_name | |
| ndc | package | 66096-125-05 | openfda.package_ndc |
| ndc | product | 66096-125 | openfda.product_ndc |
| ndc11 | package | 66096012505 | derived:openfda.package_ndc |
| spl id | d44beeee-4d22-68c3-e053-2a95a90a79ec | id | |
| spl set id | 32b7b539-ee54-4c80-a6d9-c159600927f5 | set_id | |
| unii | 387GMG9FH5 | openfda.unii | |
| unii | 00UK7646FG | openfda.unii | |
| unii | 11E6VI8VEG | openfda.unii | |
| unii | 0B4FDL9I6P | openfda.unii | |
| unii | 4QQN74LH4O | openfda.unii | |
| unii | 0YPR65R21J | openfda.unii | |
| unii | Q40Q9N063P | openfda.unii | |
| unii | 2E32821G6I | openfda.unii | |
| unii | WKC4T7680A | openfda.unii | |
| unii | 535G2ABX9M | openfda.unii | |
| unii | Y0F0BU8RDU | openfda.unii | |
| unii | J41CSQ7QDS | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.