Headek Nasal Spray
- Manufacturer
- Be Well Medical dba Richard Clement Nutrition y Be Well Homeopathics
- Effective date
- 2021-12-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 02:15:25
Label at a glance#
ProductHeadek Nasal
Active ingredientATROPA BELLADONNA, NITROGLYCERIN, ARABICA COFFEE BEAN, SODIUM CARBONATE, SODIUM CHLORIDE
Label structure8 sections
Contacts and useful links#
Websitewww.bewellhomeo.com
www.bewellhomeo.com
www.bewellhomeo.comLabel contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
ACTIVE INGREDIENTS (HPUS*): Belladonna 3X, 12X. Glonoinum 6X, 12X. Coffea 6X. Natrum Carb 6X. Natrum Mur 12X. (Relieves Headache & Migraine)
*The letters "HPUS" indicate that the components in the product are officially monographed in the Homeopathic Pharmacopeia of the United States.
INDICATIONS & USAGE SECTION
INDICATIONS: Temporarily relieves headaches and migraines.
WARNINGS SECTION
WARNINGS: If symptoms persist or worsen, a health professional should be consulted. As with any drug, if you are pregnant or nursing seek the advice of your physician before using this product. Consult a physician for use in children under 12 years of age.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep this and all medicines out of the reach of children.
DOSAGE & ADMINISTRATION SECTION
DOSAGE: Adults and children above 12 years: 1 spray in each nostril three to eight times daily. Consult a health care professional for use in children under 12 years of age.
OTHER SAFETY INFORMATION
TAMPER EVIDENT: There is a safety seal on the neck and cap of the bottle. Do not use this product if the safety seal is broken or missing.
INACTIVE INGREDIENT SECTION
INACTIVE INGREDIENTS: Demineralized Water, Sodium Chloride, Benzalkonium Chloride.
OTC - QUESTIONS SECTION
Manufactured for: Be Well Homeopathics Inc. Miami, FL 33178 • 1-877-438-3042
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NDC 66492-005-02
Be Well Homeopathics
HEADEK NASAL SPRAY
30ml
OTC - PURPOSE SECTION
Headache/Migraines
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 66492-005-02 | Headek Nasal | 30 mL in 1 BOTTLE, GLASS | SPRAY | 30 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 66492-005 | HEADEK NASAL (BELLADONNA, GLONOINUM, COFFEA, NATRUM CARB, NATRUM MUR.) SPRAY [BE WELL MEDICAL DBA RICHARD CLEMENT NUTRITION Y BE WELL HOMEOPATHICS] | 4 | Current NDC, Legacy NDC, 1 package rows | 20211230_976b9c85-68c9-46a5-9012-53cb24683b03.zip |
Products#
Every source-derived product name is available through these pages.
- Headek Nasal
- Belladonna, Glonoinum, Coffea, Natrum Carb, Natrum Mur.
- WATER
- BENZALKONIUM CHLORIDE
- ATROPA BELLADONNA
- NITROGLYCERIN
- ARABICA COFFEE BEAN
- SODIUM CARBONATE
- CARBONATE ION
- SODIUM CHLORIDE
- CHLORIDE ION
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 66492-005 | 66492-005-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | IACT |
| ATROPA BELLADONNA | WQZ3G9PF0H | ACTIB |
| NITROGLYCERIN | G59M7S0WS3 | ACTIB |
| ARABICA COFFEE BEAN | 3SW678MX72 | ACTIB |
| SODIUM CARBONATE | 45P3261C7T | ACTIB |
| SODIUM CHLORIDE | 451W47IQ8X | ACTIB |
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 |
|---|---|---|---|---|---|---|
| Headek Nasal | BELLADONNA, GLONOINUM, COFFEA, NATRUM CARB, NATRUM MUR. | Be Well Medical dba Richard Clement Nutrition y Be Well Homeopathics | 976b9c85-68c9-46a5-9012-53cb24683b03 | 2021-12-29 | Warnings | 66492-005-02 66492-005 66492000502 d44a0c64-2298-9c8f-e053-2a95a90a2bbf 976b9c85-68c9-46a5-9012-53cb24683b03 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.