Wood
Wood is an FDA drug label for the active ingredient BELLADONNA, BERBER VULG, CARDUUS MAR, CHELIDONIUM MAJ, CHOLESTERINUM, COLOCYNTHIS, KALI CARB, NAT PHOS, NITRICUM AC, NUX VOM, PLATINUM MET, SEPIA manufactured by NET Remedies administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20210119.
- Generic name
- BELLADONNA, BERBER VULG, CARDUUS MAR, CHELIDONIUM MAJ, CHOLESTERINUM, COLOCYNTHIS, KALI CARB, NAT PHOS, NITRICUM AC, NUX VOM, PLATINUM MET, SEPIA
- Manufacturer
- NET Remedies
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 61626-0105
- Application
- N/A
- Label effective
- 20210119
About this product
Wood is an FDA-registered drug product whose active ingredient is BELLADONNA, BERBER VULG, CARDUUS MAR, CHELIDONIUM MAJ, CHOLESTERINUM, COLOCYNTHIS, KALI CARB, NAT PHOS, NITRICUM AC, NUX VOM, PLATINUM MET, SEPIA. It is labelled by NET Remedies taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 61626-0105, label effective 20210119. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing BELLADONNA, BERBER VULG, CARDUUS MAR, CHELIDONIUM MAJ, CHOLESTERINUM, COLOCYNTHIS, KALI CARB, NAT PHOS, NITRICUM AC, NUX VOM, PLATINUM MET, SEPIA are most often described in connection with: temporary relief, neuro-emotional autonomic, nervous system, non phychiatric, disorders anger, related emotions, headache symptoms, billousness eye. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
INDICATIONS FOR USE: For temporary relief of the neuro-emotional (autonomic nervous system - non phychiatric) disorders of anger, resentment and related emotions. Temporary relief of headache symptoms. Billousness, eye - minor eye irritation, tears, muscle, neck, weak spine and lower extremity disorders.**
Dosage & Administration
DIRECTIONS: Spray 9-12 pumps (approximately 1/2 tsp.) directly in mouth 3 times a day or as directed by a licensed health care practicioner. When appropriate also spray externally on complaint area 3 times daily.
Warnings
WARNINGS: • If symptoms persist or worsen, seek advice of licensed health care practicioner. • If pregnant or nursing, take only on advice of licensed health care practicioner. • Keep this and all medication out of reach of children. • Keep this and all medication out of reach of children.
Recall and safety notices
5 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.
| Recall | Product | Firm | Class | Status | Reported |
|---|---|---|---|---|---|
| D-0006-2027 | Sterile Lubricant Dry Eye Relief Eye Drops, 0.5 FL OZ (15 mL); a) LEADER, DISTRIBUTED BY CARDINAL HEALTH, DUBLIN, OHIO 43017, www.myleader.com, NDC 70000-0502-1; b) Crocodile Tears, Distributed by: Crocodile Tears, Palm Beach Gardens, FL 33410, UPC: 8 67166 00000 4; c) Discount drug mart, Discount Drug Mart Food Fair, Medina, OH 44256, UPC: 0 93351 01156 6; d) exchange select, Manufactured for your Military Exchange By: K.C Pharmaceuticals, Inc., Pomona, CA 9176, UPC: 6 14299 05620 6; e) GERI CARE, Distributed by: Gericare Pharmaceuticals Corp., 1295 Towbin Ave., Lakewood, NJ 08701, NDC 57896-181-05; f) H.E.B Dry Eye, Eye Drops, MADE WITH PRIDE & CARE FOR H-E-B, SAN ANTONIO, TX 78204, UPC 0 41220 43741 2; g) Harris Teeter, PROUDLY DISTRIBUTED BY: HARRIS TEETER, LLC, MATTHEWS, NC 28105, UPC: 0 72036 71303 2; h) Foster & Thrive, Distributed by: McKesson Corp. Via Strategic Sourcing Servies LLC., Memphis, TN 38141, NDC 70677-1157-1; I) TopCare health, DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELKGROVE VILLAGE, IL 60007, UPC 0 36800 36100 3. | K.C. Pharmaceuticals, Inc. | Class II | Ongoing | 20261014 |
| D-0835-2026 | Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL per dropper bottle, For Office Use Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-732-10 | ImprimisRx NJ LLC | Class III | Ongoing | 20260916 |
| D-0731-2026 | Azelaic Acid Gel, 15%, 50 gram tubes, For Topical Use only, Rx only, Distributed by: Glenmark Pharmaceuticals Inc., USA, Elmwood Park, NJ 07407, NDC 68462-626-52. | Glenmark Pharmaceuticals Inc., USA | Class II | Ongoing | 20260805 |
| D-0683-2026 | FAMILY Wellness, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), Kit - Washer Bulb Included, (NDC 55319-835-01), DISTRIBUTED BY: MIDWOOD BRANDS LLC, 500 VOLVO PKWY, CHESAPEAKE, VA 23320. | Bell Pharmaceuticals, Inc | Class II | Ongoing | 20260722 |
| D-0569-2026 | FAMILY WELLNESS, ULTRA STRENGT, ANTACID TABLETS, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, DISTRIBUTED BY: MIDWOOD BRANDS, LLC, 500 VOLVO PKWY, CHESAPEAKE, VA 23320 USA., UP: 0 32251-92282-4. | Guardian Drug Co. Inc. | Class II | Ongoing | 20260610 |
Frequently asked questions
What is Wood used for?
INDICATIONS FOR USE: For temporary relief of the neuro-emotional (autonomic nervous system - non phychiatric) disorders of anger, resentment and related emotions. Temporary relief of headache symptoms. Billousness, eye - minor eye irritation, tears, muscle, neck, weak spine and lower extremity disorders.**
Who makes Wood?
NET Remedies is the labeler of record for Wood.
What form does Wood come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Wood prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has Wood been recalled?
5 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.