warnings
Warnings Stop use and consult a doctor if symptoms worsen or persist for more than 7 days. If pregnant or breast-feeding, ask a healthcare professional before use.
Snore 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
- Snore Control
- Generic name
- BROMIUM, CHAMOMILLA, CINCHONA, CUPRUM METALLICUM, HELLEBORUS NIGER, HISTAMINUM HYDROCHLORICUM, HYDRASTIS CANADENSIS, KALI BICHROMICUM, LAUROCERASUS, NUX VOMICA, PHOSPHORICUM ACIDUM, RHUS TOX, SILICEA, STRAMONIUM, SULPHUR AND ZINCUM METALLICUM.
- Manufacturer
- King Bio Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 704bb574-6c54-49d1-bdae-81ffe0e79d10
- SPL ID
- 6f361b61-60c1-4c90-8121-59b1a47c2197
- Version
- 1
- Effective date
- 2026-03-04
- Source export date
- 2026-11-06
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:50:18
| 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 | Snore Control | openfda.brand_name | |
| generic name | BROMIUM, CHAMOMILLA, CINCHONA, CUPRUM METALLICUM, HELLEBORUS NIGER, HISTAMINUM HYDROCHLORICUM, HYDRASTIS CANADENSIS, KALI BICHROMICUM, LAUROCERASUS, NUX VOMICA, PHOSPHORICUM ACIDUM, RHUS TOX, SILICEA, STRAMONIUM, SULPHUR AND ZINCUM METALLICUM. | openfda.generic_name | |
| manufacturer name | King Bio Inc. | openfda.manufacturer_name | |
| ndc | package | 57955-9983-2 | openfda.package_ndc |
| ndc | product | 57955-9983 | openfda.product_ndc |
| ndc11 | package | 57955998302 | derived:openfda.package_ndc |
| spl id | 6f361b61-60c1-4c90-8121-59b1a47c2197 | id | |
| spl set id | 704bb574-6c54-49d1-bdae-81ffe0e79d10 | set_id | |
| unii | 789U1901C5 | openfda.unii | |
| unii | SBV4XY874G | openfda.unii | |
| unii | 269XH13919 | openfda.unii | |
| unii | 3POA0Q644U | openfda.unii | |
| unii | 608DGJ6815 | openfda.unii | |
| unii | F26P2D4757 | openfda.unii | |
| unii | ETJ7Z6XBU4 | openfda.unii | |
| unii | 6IO182RP7A | openfda.unii | |
| unii | ZW3Z11D0JV | openfda.unii | |
| unii | S003A158SB | openfda.unii | |
| unii | 70FD1KFU70 | openfda.unii | |
| unii | G6W4F0V8Z3 | openfda.unii | |
| unii | T4423S18FM | openfda.unii | |
| unii | E4GA8884NN | openfda.unii | |
| unii | G0R4UBI2ZZ | 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.