Dermapar
Epidermis (Suis), Arsenicum Album, Calcarea Carbonica, Graphites, Mezereum, Natrum Muriaticum, Nitricum Acidum, Petroleum, Rhus Tox, Sulphur, Causticum · Liquid · Oral
Active ingredient
ACTIVE INGREDIENT: (in each drop): 9.99% of Arsenicum Album 12X, Calcarea Carbonica 12X, Causticum 30X, Graphites 12X, Mezereum12X, Natrum Muriaticum 12X, Nitricum Acidum 12X, Petroleum 12X, Rhus Tox 12X, Sulphur 12X; 0.10% of Epidermis 6X.
Purpose
INDICATIONS: May temporarily relieve itching, burning, weeping, cracks and eruptions.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Uses
INDICATIONS: May temporarily relieve itching, burning, weeping, cracks and eruptions.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Warnings
WARNINGS: 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 contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.
Keep out of reach of children
KEEP OUT OF REACH OF CHILDREN: In case of overdose, get medical help or contact a Poison Control Center right away.
Directions
DIRECTIONS: Adults and children 5 to 10 drops orally, 3 time daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.
Inactive ingredients
INACTIVE INGREDIENTS: Demineralized water, 20% Ethanol.
Questions?
QUESTIONS: Dist. by Energique, Inc. 201 Apple Blvd Woodbine, IA 51579 800-869-8078
Label text from the FDA structured product label by Energique, Inc. (revised Apr 22, 2024). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Sus Scrofa Skin in 1 product
- Arsenic Trioxide in 1 product
- Oyster Shell Calcium Carbonate, Crude in 1 product
- Graphite in 1 product
- Daphne Mezereum Bark in 1 product
- Sodium Chloride in 1 product
- Nitric Acid in 1 product
- Kerosene in 1 product
- Toxicodendron Pubescens Leaf in 1 product
- Sulfur in 1 product
- Causticum in 1 product
Dermapar NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 44911-0562 | Sus Scrofa Skin 6 [hp_X]/mL; Arsenic Trioxide 12 [hp_X]/mL; Oyster Shell Calcium Carbonate, Crude 12 [hp_X]/mL;… Liquid | Energique, Inc. | UNAPPROVED HOMEOPATHIC |
Frequently asked questions
What is Dermapar used for?
INDICATIONS: May temporarily relieve itching, burning, weeping, cracks and eruptions.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Who makes Dermapar?
Dermapar is listed by 1 labeler in the FDA NDC directory, including Energique, Inc..