Otc - Active Ingredient
Aconitum Napellus, 24X HPUS
Hypericum Peforatum, 24X HPUS
Lycopodium Clavatum, 24X HPUS
Phosphorus, 24X HPUS
Rhus Toxicodendron, 24X HPUS
Secale Cornuum, 24X HPUS
Pain Away Solution
FDA Label NDC 65121-887
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Pure Source, Llc for the product Pain Away Solution (NDC 65121-887). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Nerve Pain Relief
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away - (800-222-1222)
Indications & Usage
Use
For the temporary relief of nerve pain
Warnings
Warnings
For external use only.
Do not use on wounds or damaged skin.
Stop use and ask doctor if
- Symptoms persist for more than seven days.
- If irritation occurs, discontinue use.
- Avoid contact with eyes.
- Do not wrap treated area with bandage.
When using this product
If pregnant or breast feeding, ask a health professional before use.
Dosage & Administration
Directions
- Spray small amount to cover the affected area.
- Do not apply more than 4 times daily.
- Avoid contact with eyes and mucus membranes.
Inactive Ingredient
Inactive Ingredients
Bergamot Oil, Cassia Leaf Oil, Eucalyptus Oil, Geranium Oil, Histamine Dihydrochloride, Lavender Oil, Safflower Oil, SD-Alcohol 38B, Tea Tree Oil
* Please review the disclaimer below.
