warnings
Warnings Keep out of the reach of children. If pregnant or breast-feeding, ask a health care professional before use.Stop use and ask a health care professional if symptoms persist for more than 3 days or worsen.
Throat Remedy
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
- Throat Remedy
- Generic name
- BELLADONNA 30C, HEAR SULPHURIS CALCAREUM 30C, LACHESIS MUTUS 30C, MERCURIUS SOLUBILIS 30C, PHYTOLACCA DECANDRA 30C, FERRUM PHOSPHORICUM 6X, KALI MURIATICUM 5X, CALCAREA SULPHURICA 6X, STREPTOCOCCINUM 200C
- Manufacturer
- JoyWell Co LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 51c00f80-3642-4552-a0f8-02a0f7495cf8
- SPL ID
- 45ac48ac-6ac0-dd2b-e063-6394a90a10b5
- Version
- 1
- Effective date
- 2025-12-11
- Source export date
- 2026-10-12
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:39:33
| 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 | Throat Remedy | openfda.brand_name | |
| generic name | BELLADONNA 30C, HEAR SULPHURIS CALCAREUM 30C, LACHESIS MUTUS 30C, MERCURIUS SOLUBILIS 30C, PHYTOLACCA DECANDRA 30C, FERRUM PHOSPHORICUM 6X, KALI MURIATICUM 5X, CALCAREA SULPHURICA 6X, STREPTOCOCCINUM 200C | openfda.generic_name | |
| manufacturer name | JoyWell Co LLC | openfda.manufacturer_name | |
| ndc | package | 85946-0002-1 | openfda.package_ndc |
| ndc | product | 85946-0002 | openfda.product_ndc |
| ndc11 | package | 85946000201 | derived:openfda.package_ndc |
| spl id | 45ac48ac-6ac0-dd2b-e063-6394a90a10b5 | id | |
| spl set id | 51c00f80-3642-4552-a0f8-02a0f7495cf8 | set_id | |
| unii | N6BAA189V1 | openfda.unii | |
| unii | 11E6VI8VEG | openfda.unii | |
| unii | LJ2LP0YL98 | openfda.unii | |
| unii | WAT0DDB505 | openfda.unii | |
| unii | 660YQ98I10 | openfda.unii | |
| unii | WQZ3G9PF0H | openfda.unii | |
| unii | J78005WL7R | openfda.unii | |
| unii | VSW71SS07I | openfda.unii | |
| unii | 1MBW07J51Q | 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.