Pain 200 [hp_C]/mL
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 · SPRAY · Liddell Laboratories, Inc.
Pain is a spray 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 at 200 [hp_C]/mL, taken oral. Manufactured by Liddell Laboratories, Inc..
Key Facts
- Brand Name
- Pain
- 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
- NDC Code (Product)
50845-0265- Manufacturer
- Liddell Laboratories, Inc.
- Strength
- 200 [hp_C]/mL
- Dosage Form
- SPRAY
- Route
- ORAL
- Marketing Status
- Drug Class
- Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]
- Marketing Start
- 03/26/2020
Recall History
Sentara Infusion Services
Lack of sterility assurance
Ecometics, Inc.
CGMP DEVIATIONS
Ideaz Llc
CGMP Deviations: Products manufactured with an ingredient that exceed the benzene levels allowed in drug products.
Contract Pharmacal Corporation
Presence of Foreign Tablets/Capsules: Complaint involving one Women's Prenatal dietary supplement tablet commingled in a bottle of Extra Strength Acetaminophen 500 mg contents 1000 count bottle.
ARG Laboratories, Inc.
Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Reckitt Benckiser LLC
Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing certain Active Ingredients such as acetaminophen, phenylephrine, dextromethorphan, diphenhydramine, and/or guaifenesin. As a result certain safety warnings associated with those ingredients may also be missing.
Ultra Seal Corporation
cGMP deviations
Ridge Properties, LLC
Microbial Contamination of Non-Sterile Products: products were found to be contaminated and above specification for lidocaine assay.
Ridge Properties, LLC
GMP Deviations: inadequate manufacturing control processes
Humco Holding Group, Inc
Microbial Contamination of Non-Sterile Product(s): The product was found to be contaminated with Bulkholderia sp.
Side Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Full Prescribing Information
Indications & Usage
Uses temporarily relieves minor aches and pains due to: headache the common cold backache minor pain of arthritis toothache muscular aches premenstrual and menstrual cramps temporarily reduces fever
Dosage & Administration
Directions do not take more than directed adults and children 12 years and over take 2 gelcaps every 6 hours while symptoms last do not take more than 6 gelcaps in 24 hours, unless directed by a doctor do not take for more than 10 days unless directed by a doctor children under 12 years: ask a doctor
Warnings
Warnings Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take more than 4,000 mg of acetaminophen in 24 hours with other drugs containing acetaminophen 3 or more alcoholic drinks every day while using this product Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include: skin reddening blisters rash If a skin reaction occurs, stop use and seek medical help right away. Do not use if you are allergic to acetaminophen or any of the inactive ingredients in this product with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. Ask a doctor before use if you have liver disease. Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin. Stop use and ask a doctor if new symptoms occur pain gets worse or lasts more than 10 days fever gets worse or lasts more than 3 days redness or swelling is present These could be signs of a serious condition. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or cont…
Frequently Asked Questions
What is Pain used for?
Pain contains 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 a spray taken oral. Consult your doctor for specific uses.
Is Pain a controlled substance?
Pain is not classified as a controlled substance by the DEA.
What is the generic name for Pain?
The generic name for Pain 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. There are no other listed brand versions of 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.
What is the NDC code for Pain 200 [hp_C]/mL?
The NDC (National Drug Code) for Pain 200 [hp_C]/mL is 50845-0265, listed by Liddell Laboratories, Inc..
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)