Dosage and administration
Adults and children over 12: Spray liberally on affected area as needed. Children 12 and under: Consult a doctor prior to use. Shake well before use.
Derma Pain
- Manufacturer
- Liddell Laboratories, Inc. | Apotheca Company
- Effective date
- 2024-11-04
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:28:48
Label at a glance#
ProductDerma Pain
Active ingredientCALENDULA OFFICINALIS FLOWERING TOP, CROTON TIGLIUM SEED, SODIUM CHLORIDE, PLANTAGO MAJOR WHOLE, TOXICODENDRON PUBESCENS LEAF, SMILAX ORNATA ROOT
Label structure9 sections
Contacts and useful links#
Websitewww.liddell.net
WWW.LIDDELL.NET
WWW.LIDDELL.NETLabel contents#
Full prescribing information#
ACTIVE INGREDIENTS:
(in each spray) 0.21% of Calendula Officinalis 12X, Croton Tiglium 30X, Natrum Muriaticum 30X, Plantago Major 30X, Rhus Tox 30X, Sarsaparilla (Smilax Regelii) 30X.
INDICATIONS:
May temporarily relieve shooting pain, itching, burning, and sensitivity to touch, with or after eruptions and blisters.**
**Clains based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
WARNINGS:
For external use only.
If symptoms persist for more than 7 days, consult a doctor.
If pregnant or breast feeding, ask a health professional before use.
Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center right away.
Do not get into eyes
Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.
KEEP OUT OF REACH OF CHILDREN:
Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center right away.
DIRECTIONS:
Adults and children over 12: Spray liberally on affected area as needed. Children 12 and under: Consult a doctor prior to use.
Shake well before use.
INDICATIONS:
May temporarily relieve shooting pain, itching, burning, and sensitivity to touch, with or after eruptions and blisters.**
**Clains based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
INACTIVE INGREDIENTS:
Aloe Vera Leaf Juice, Arnica Flower*, Chaparral Leaf*, Citric Acid, Comfrey Leaf*, Dragon's Blood Croton (Sap), English Lavender (Buds)*, Ethanol, Ionic Colloidal Silver, Lemon Balm Leaf*, PEG-33, PEG-8 Dimethicone, PEG-14, Phenoxyethanol, Caprylyl Glycol, Sorbic Acid, Poke Berries*, Poke Root*, Potassium Sorbate, Purified Water, Sodium Bicarbonate, St. John's Wort Aerial Parts, Tocopherols (Vitamin E Oil), Vitamin C, Whey Protein Concentrate, White Willow Bark*, Yarrow Flower*.
QUESTIONS:
PACKAGE LABEL DISPLAY:
TOPICAL SPRAYS
LIDDELL
LABORATORIES
EST 1994
Derma Pain
TOPICAL HOMEOPATHIC SPRAY
1.0 FL. OZ. (30 ml)
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50845-0280-1 | Derma Pain | 30 mL in 1 BOTTLE, SPRAY | SPRAY | 30 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50845-0280 | DERMA PAIN (CALENDULA OFFICINALIS, CROTON TIGLIUM, NATRUM MURIATICUM, PLANTAGO MAJOR, RHUS TOX, SARSAPARILLA (SMILAX REGELII)) SPRAY [LIDDELL LABORATORIES, INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20241106_e02a5e99-aa27-4276-a785-7b5328d89fdc.zip |
Products#
Every source-derived product name is available through these pages.
- Derma Pain
- Calendula Officinalis, Croton Tiglium, Natrum Muriaticum, Plantago Major, Rhus Tox, Sarsaparilla (Smilax Regelii)
- CALENDULA OFFICINALIS FLOWERING TOP
- CROTON TIGLIUM SEED
- SODIUM CHLORIDE
- CHLORIDE ION
- PLANTAGO MAJOR WHOLE
- PLANTAGO MAJOR
- TOXICODENDRON PUBESCENS LEAF
- SMILAX ORNATA ROOT
- SARSAPARILLA
- ALOE VERA LEAF
- ARNICA MONTANA FLOWER
- LARREA TRIDENTATA LEAF
- CITRIC ACID MONOHYDRATE
- COMFREY LEAF
- CROTON LECHLERI RESIN
- LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER
- ALCOHOL
- SILVER
- MELISSA OFFICINALIS LEAF
- POLYETHYLENE GLYCOL 1600
- PEG-8 DIMETHICONE
- POLYETHYLENE GLYCOL 700
- PHENOXYETHANOL
- CAPRYLYL GLYCOL
- SORBIC ACID
- PHYTOLACCA AMERICANA FRUIT
- PHYTOLACCA AMERICANA ROOT
- POTASSIUM SORBATE
- WATER
- SODIUM BENZOATE
- SODIUM BICARBONATE
- HYPERICUM PERFORATUM
- .ALPHA.-TOCOPHEROL
- ASCORBIC ACID
- WHEY
- SALIX ALBA BARK
- ACHILLEA MILLEFOLIUM FLOWER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50845-0280 | 50845-0280-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| Derma Pain | CALENDULA OFFICINALIS, CROTON TIGLIUM, NATRUM MURIATICUM, PLANTAGO MAJOR, RHUS TOX, SARSAPARILLA (SMILAX REGELII) | Liddell Laboratories, Inc. | e02a5e99-aa27-4276-a785-7b5328d89fdc | 2024-11-04 | Warnings | 50845-0280-1 50845-0280 50845028001 f378a799-7c5f-45bf-a78b-1f9617f30121 e02a5e99-aa27-4276-a785-7b5328d89fdc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.