Pain
Pain is an FDA drug label for the active ingredient ACONITUM NAPELLUS, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA (ALBA), CARTILAGO SUIS, CAUSTICUM, CHAMOMILLA, COFFEA CRUDA, EUPHORBIUM OFFICINARUM, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, MAGNESIA PHOSPHORICA, PASSIFLORA INCARNATA, PYROGENIUM, RANUNCULUS BULBOSUS, SYMPHYTUM OFFICINALE manufactured by Liddell Laboratories, Inc. 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 20231219.
- Generic name
- ACONITUM NAPELLUS, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA (ALBA), CARTILAGO SUIS, CAUSTICUM, CHAMOMILLA, COFFEA CRUDA, EUPHORBIUM OFFICINARUM, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, MAGNESIA PHOSPHORICA, PASSIFLORA INCARNATA, PYROGENIUM, RANUNCULUS BULBOSUS, SYMPHYTUM OFFICINALE
- Manufacturer
- Liddell Laboratories, Inc.
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 50845-0265
- Application
- N/A
- Label effective
- 20231219
About this product
Pain is an FDA-registered drug product whose active ingredient is ACONITUM NAPELLUS, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA (ALBA), CARTILAGO SUIS, CAUSTICUM, CHAMOMILLA, COFFEA CRUDA, EUPHORBIUM OFFICINARUM, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, MAGNESIA PHOSPHORICA, PASSIFLORA INCARNATA, PYROGENIUM, RANUNCULUS BULBOSUS, SYMPHYTUM OFFICINALE. It is labelled by Liddell Laboratories, Inc. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 50845-0265, label effective 20231219. 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 ACONITUM NAPELLUS, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA (ALBA), CARTILAGO SUIS, CAUSTICUM, CHAMOMILLA, COFFEA CRUDA, EUPHORBIUM OFFICINARUM, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, MAGNESIA PHOSPHORICA, PASSIFLORA INCARNATA, PYROGENIUM, RANUNCULUS BULBOSUS, SYMPHYTUM OFFICINALE are most often described in connection with: temporarily relieve, minor aches, pains claims, based traditional, homeopathic practice, accepted medical, fda evaluated. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
INDICATIONS: May temporarily relieve minor aches and pains.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Dosage & Administration
DIRECTIONS: Adults and children over 12: Spray twice under the tongue every 30 minutes until symptoms are relieved. Children 12 and under: Consult a doctor prior to use.
Warnings
WARNINGS: If symptoms persist for more than 7 days, 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.
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-0829-2026 | Broadway Joe's Pain Cream, 3000 gm CBD, (Histamine Dihydrochloride 0.025%) (CDB Isolate 3000mg, HempSeed Oil 2000mg),4 oz-jar, Produced for Broadway Joe's, Franklin, TN, 37067, NDC 83088-8120-6; UPC 8 50041 64004 4 | Lexia LLC | Class II | Ongoing | 20260909 |
| D-0828-2026 | Broadway Joe's Pain Cream, (Histamine Dihydrochloride 0.025%), 1500mg CBD Isolate, 1000mg Hempseed oil, 2 oz-jar, Produced for Broadway Joe's, Franklin, TN, 37067, NDC 83088-8120-5, UPC 8 50041 64003 7 | Lexia LLC | Class II | Ongoing | 20260909 |
| D-0582-2026 | Duloxetine Delayed-Release Capsules, USP, 30mg, 1000 Capsule bottles, Rx only, Manufactured. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Distributed by: Breckenridge Pharmaceuticals, Inc., Berkeley Heights, NJ 07922. NDC 51991-747-10 | Breckenridge Pharmaceutical, Inc. | Class II | Ongoing | 20260617 |
| D-0583-2026 | Duloxetine Delayed-Release Capsules, USP, 60mg, packaged in a) 90 Capsules (NDC 51991-748-90); b) 1000 Capsules (51991-748-10), Rx Only, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Dist. by: Breckenridge Pharmaceuticals, Inc., Berkeley Heights, NJ 07922. | Breckenridge Pharmaceutical, Inc. | Class II | Ongoing | 20260617 |
| D-0522-2026 | Duloxetine Delayed-Release Capsules USP, 60mg, Rx Only, 90-count bottle, Mfr. by Towa Pharmaceutical Eurpoe S.L., Martorelles, (Barcelona), Spain, Dist. by. Breckenridge Pharmaceutical, Inc., Berkely Heights, NJ 07922, NDC 51991-748-90. | Breckenridge Pharmaceutical, Inc. | Class II | Ongoing | 20260513 |
Frequently asked questions
What is Pain used for?
INDICATIONS: May temporarily relieve minor aches and pains.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Who makes Pain?
Liddell Laboratories, Inc. is the labeler of record for Pain.
What form does Pain 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 Pain 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 Pain 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.