PAIN RELIEF
- Manufacturer
- NET Remedies
- Effective date
- 2021-01-19
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:14:12
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
ACTIVE INGREDIENTS (HPUS*): Contains equal volumes of each in 12X, 30X, and 100X potencies: Arnica, Chamomilla, Hypericum, Ignatia, Symphytum.
(*) The letters "HPUS" indicate that the components in the product are officially monographed in the Homeopathic Pharmacopeia of the United States.
(**) Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
INDICATIONS & USAGE SECTION
INDICATIONS FOR USE: For the temporary relief of general pain, includingm symptoms related to joints, bones, muscles, minor bruises, spinal pain and pain due to arthiritis. **
WARNINGS SECTION
WARNINGS:
• If symptoms persist or worsen, seek advice of licensed health care practitioner.
• If pregnant or nursing, take on only advice of licensed health care practitioner.
• Keep this and all medication out of reach of children.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
• Keep this and all medication out of reach of children.
DOSAGE & ADMINISTRATION SECTION
DIRECTIONS: Spray 9-12 pumps (approximately 1/2 tsp.) directly in mouth 3 times a day or as directed by a licensed health care practitioner. When appropriate, also spray externally on complaint area 3 times daily.
OTHER SAFETY INFORMATION
OTHER INFORMATION: Tamper resistant for your protection. Use only if safety seal is intact.
INACTIVE INGREDIENT SECTION
INACTIVE INGREDIENTS: Citric acid, Potassium sorbate, Purified water.
Free of Alcohol, Sugar, Sodium, Yeast and Gluten
OTC - QUESTIONS SECTION
Made in the USA
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NET Remedies #20
PAIN RELIEF
Homeopathic Preparation
PROFESSIONAL FORMULA
Naturally No Side Effects
2 fl oz (59 mL)
OTC - PURPOSE SECTION
INDICATIONS FOR USE: For the temporary relief of general pain, includingm symptoms related to joints, bones, muscles, minor bruises, spinal pain and pain due to arthiritis. **
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 61626-0099-4 | PAIN RELIEF | 59 mL in 1 BOTTLE | LIQUID | 59 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 61626-0099 | PAIN RELIEF (ARNICA, CHAMOMILLA, HYPERICUM, IGNATIA, SYMPHYTUM) LIQUID [NET REMEDIES] | 2 | Current NDC, Legacy NDC, 1 package rows | 20210121_75786c15-be49-4548-8f7a-319f86aa0cee.zip |
Products#
Every source-derived product name is available through these pages.
- PAIN RELIEF
- Arnica, Chamomilla, Hypericum, Ignatia, Symphytum
- CITRIC ACID MONOHYDRATE
- POTASSIUM SORBATE
- WATER
- ARNICA MONTANA
- MATRICARIA CHAMOMILLA
- HYPERICUM PERFORATUM
- STRYCHNOS IGNATII SEED
- COMFREY ROOT
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 61626-0099 | 61626-0099-4 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| POTASSIUM SORBATE | 1VPU26JZZ4 | IACT |
| WATER | 059QF0KO0R | IACT |
| ARNICA MONTANA | O80TY208ZW | ACTIB |
| MATRICARIA CHAMOMILLA | G0R4UBI2ZZ | ACTIB |
| HYPERICUM PERFORATUM | XK4IUX8MNB | ACTIB |
| STRYCHNOS IGNATII SEED | 1NM3M2487K | ACTIB |
| COMFREY ROOT | M9VVZ08EKQ | 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 |
|---|---|---|---|---|---|---|
| PAIN RELIEF | ARNICA, CHAMOMILLA, HYPERICUM, IGNATIA, SYMPHYTUM | NET Remedies | 75786c15-be49-4548-8f7a-319f86aa0cee | 2021-01-19 | Warnings | 61626-0099-4 61626-0099 61626009904 b9492b5a-9070-4f3c-e053-2a95a90a6650 75786c15-be49-4548-8f7a-319f86aa0cee |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
