Dermapain HP by Energique, Inc / Apotheca Company Drug Facts:

Dermapain HP by

Drug Labeling and Warnings

Dermapain HP by is a Homeopathic medication manufactured, distributed, or labeled by Energique, Inc, Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DERMAPAIN HP- echinacea (angustifolia), kali phosphoricum, sarracenia purpurea, arsenicum album, causticum, dolichos pruriens, hypericum perforatum, mezereum, ranunculus bulbosus, rhus tox liquid 
Energique, Inc

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Drug Facts:

ACTIVE INGREDIENTS:

(in each drop): 10% of Arsenicum Album 30X, Causticum 30X, Dolichos Pruriens 30X, Echinacea (Angustifolia) 6X, Hypericum Perforatum 30X, Kali Phosphoricum 6X, Mezereum 30X, Ranunculus Bulbosus 30X, Rhus Tox 30X, Sarracenia Purpurea 9X.

INDICATIONS:

May temporarily relieve minor symptoms of shooting pain, itching, burning, and sensitivity to touch with or after eruptions and blisters.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

If pregnant or breastfeeding, 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:

Adults and children 5 to 10 drops orally, 3 times 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.

INDICATIONS:

May temporarily relieve minor symptoms of shooting pain, itching, burning, and sensitivity to touch with or after eruptions and blisters.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENTS:

Demineralized water, 20% Ethanol

QUESTIONS:

Dist. by Energique, Inc.
201 Apple Blvd.
Woodbine, IA 51579 800.868.8078

PACKAGE LABEL DISPLAY:

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

DERMAPAIN HP

1 fl. oz. (30 ml)

DERMAPAIN HP 
echinacea (angustifolia), kali phosphoricum, sarracenia purpurea, arsenicum album, causticum, dolichos pruriens, hypericum perforatum, mezereum, ranunculus bulbosus, rhus tox liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44911-0568
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8)	ECHINACEA ANGUSTIFOLIA	6 [hp_X]  in 1 mL
POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR)	POTASSIUM PHOSPHATE, DIBASIC	6 [hp_X]  in 1 mL
SARRACENIA PURPUREA (UNII: FOP08H143P) (SARRACENIA PURPUREA - UNII:FOP08H143P)	SARRACENIA PURPUREA	9 [hp_X]  in 1 mL
ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV)	ARSENIC TRIOXIDE	30 [hp_X]  in 1 mL
CAUSTICUM (UNII: DD5FO1WKFU) (CAUSTICUM - UNII:DD5FO1WKFU)	CAUSTICUM	30 [hp_X]  in 1 mL
MUCUNA PRURIENS FRUIT TRICHOME (UNII: 3E271BSI0C) (MUCUNA PRURIENS FRUIT TRICHOME - UNII:3E271BSI0C)	MUCUNA PRURIENS FRUIT TRICHOME	30 [hp_X]  in 1 mL
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB)	HYPERICUM PERFORATUM	30 [hp_X]  in 1 mL
DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (DAPHNE MEZEREUM BARK - UNII:X2N6E405GV)	DAPHNE MEZEREUM BARK	30 [hp_X]  in 1 mL
RANUNCULUS BULBOSUS (UNII: AEQ8NXJ0MB) (RANUNCULUS BULBOSUS - UNII:AEQ8NXJ0MB)	RANUNCULUS BULBOSUS	30 [hp_X]  in 1 mL
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A)	TOXICODENDRON PUBESCENS LEAF	30 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44911-0568-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	05/24/2021	09/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		05/24/2021	09/01/2022

Labeler - Energique, Inc (789886132)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(44911-0568) , api manufacture(44911-0568) , label(44911-0568) , pack(44911-0568)

Revised: 5/2022

Document Id: a2635144-a028-44d0-b11b-abd680cf5dfc

34390-5

Set id: 2b8a4ef5-d535-4551-9971-0af10c524c3f

Version: 2

Effective Time: 20220523