Dosage and administration
Adults: Spray twice under the tongue 3 times per day, with last dose at bedtime and additional doses whenever sleep is interrupted.
Snore Defense
- Manufacturer
- Liddell Laboratories | Apotheca Company
- Effective date
- 2021-12-21
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:21:36
Label at a glance#
ProductSnore Defense
Active ingredientANTIMONY POTASSIUM TARTRATE, ACTIVATED CHARCOAL, GRINDELIA HIRSUTULA FLOWERING TOP, SUS SCROFA LUNG, SUS SCROFA NASAL MUCOSA, STRYCHNOS NUX-VOMICA SEED, ASPIDOSPERMA QUEBRACHO-BLANCO BARK, LOBARIA PULMONARIA, TEUCRIUM MARUM
Label structure9 sections
Contacts and useful links#
Websitewww.liddell.net
WWW.LIDDELL.NET
WWW.LIDDELL.NETLabel contents#
Full prescribing information#
ACTIVE INGREDIENTS:
Antimonium tartaricum 200C, Carbo vegetabilis 12X, Grindelia (Robusta) 200C, Lung suis 6X, Mucosa nasalis suis 6X, Nux vomica 12X, Quebracho 3X, Sticta pulmonaria 200C, Teucrium marum 3X.
INDICATIONS:
May help reduce the loudness and frequency of snoring and may promote a more restful night's sleep.**
**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
WARNINGS:
Persons who have symptoms of sleep apnea should consult a doctor.
If pregnant or breast feeding, ask a doctor before use.
Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.
Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.
KEEP OUT OF REACH OF CHILDREN:
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
DIRECTIONS:
Adults: Spray twice under the tongue 3 times per day, with last dose at bedtime and additional doses whenever sleep is interrupted.
INDICATIONS:
May help reduce the loudness and frequency of snoring and may promote a more restful night's sleep.**
**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
INACTIVE INGREDIENTS:
Organic alcohol 20% v/v, Purified water.
QUESTIONS:
PACKAGE LABEL DISPLAY:
ORAL SPRAYS
LIDDELL
LABORATORIES
EST. 1994
57SN-
Snore Defense
HOMEOPATHIC
1.0 FL. OZ. (30 ML)
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50845-0251-1 | 2021-12-21 | C162847 | 48780-1 | ba0f9c33-4e3e-a910-e053-dadaa90a0b85 | Drug Facts: |
| 50845-0251-1 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-4e3e-a910-e053-dadaa90a0b85 | Drug Facts: |
Products#
Every source-derived product name is available through these pages.
- Snore Defense
- Antimonium tartaricum, Carbo vegetabilis, Grindelia (Robusta), Lung suis, Mucosa nasalis suis, Nux vomica, Quebracho, Sticta pulmonaria, Teucrium marum
- ANTIMONY POTASSIUM TARTRATE
- ANTIMONY CATION (3+)
- ACTIVATED CHARCOAL
- GRINDELIA HIRSUTULA FLOWERING TOP
- SUS SCROFA LUNG
- SUS SCROFA NASAL MUCOSA
- STRYCHNOS NUX-VOMICA SEED
- ASPIDOSPERMA QUEBRACHO-BLANCO BARK
- LOBARIA PULMONARIA
- TEUCRIUM MARUM
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50845-0251 | 50845-0251-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ANTIMONY POTASSIUM TARTRATE | DL6OZ476V3 | ACTIB |
| ACTIVATED CHARCOAL | 2P3VWU3H10 | ACTIB |
| GRINDELIA HIRSUTULA FLOWERING TOP | IDB0NAZ6AI | ACTIB |
| SUS SCROFA LUNG | 7GL3G1COB3 | ACTIB |
| SUS SCROFA NASAL MUCOSA | ID3Z1X61WY | ACTIB |
| STRYCHNOS NUX-VOMICA SEED | 269XH13919 | ACTIB |
| ASPIDOSPERMA QUEBRACHO-BLANCO BARK | 52B1340190 | ACTIB |
| LOBARIA PULMONARIA | D1YM0P5Z2T | ACTIB |
| TEUCRIUM MARUM | 10464S0TAA | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | 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 |
|---|---|---|---|---|---|---|
| df521eee-ede6-4a79-96de-ce9b70d4be45 | 316a23ca-be7f-4e97-99b1-b3a2e84efa96 | 2021-12-21 | Warnings | df521eee-ede6-4a79-96de-ce9b70d4be45 316a23ca-be7f-4e97-99b1-b3a2e84efa96 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.