ABROPERNOL- artemisia abrotanum flowering top and pulsatilla vulgaris and calcium fluoride and hamamelis virginiana root bark/stem bark and amanita muscaria var. muscaria fruiting body and nitric acid and kerosene tablet

Abropernol by

Drug Labeling and Warnings

Abropernol by is a Homeopathic medication manufactured, distributed, or labeled by Heel Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

KEEP OUT OF REACH OF CHILDREN

Keep this and all medications out of the reach of children.

INDICATIONS AND USAGE

For the temporary relief of:

• Dermatitus
• Minor skin irritations
• Eczema, hyperhidrosis
• Hyperkeratosis
  

WARNINGS

If symptoms persist or worsen, a physician should be consulted. As with any drug, if you are pregnant or nursing a baby, seek the advise of a health care professional before using this product.

DOSAGE AND ADMINISTRATION

Adults and children above 6 years: 1 tablet sublingually or dissolved completely in mouth 3 times daily or as directed by a physician.
Infants and children to 6 years: 1/2 the adult dosage.

ACTIVE INGREDIENT

Each 300mg tablet contains as active ingredients: Abrotanum 4X, Pulsatilla 4X, Calcarea fluorica 12X 60 mg each; Hamamelis virginiana 4X, Agaricus muscarius 5X, Nitricum acidum 6X, Petroleum 6X 30 mg each.

INACTIVE INGREDIENT

Inactive ingredients: Lactose, Magnesium Stearate

PURPOSE

Dermatitus, Minor skin irritations, Eczema, hyperhidrosis, Hyperkeratosis

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ABROPERNOL 
artemisia abrotanum flowering top and pulsatilla vulgaris and calcium fluoride and hamamelis virginiana root bark/stem bark and amanita muscaria var. muscaria fruiting body and nitric acid and kerosene tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50114-6134
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0) (ARTEMISIA ABROTANUM FLOWERING TOP - UNII:QG07G580U0)	ARTEMISIA ABROTANUM FLOWERING TOP	4 [hp_X]  in 300 mg
PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV)	PULSATILLA VULGARIS	4 [hp_X]  in 300 mg
CALCIUM FLUORIDE (UNII: O3B55K4YKI) (CALCIUM FLUORIDE - UNII:O3B55K4YKI)	CALCIUM FLUORIDE	12 [hp_X]  in 300 mg
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - UNII:T7S323PKJS)	HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK	4 [hp_X]  in 300 mg
AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY (UNII: DIF093I037) (AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY - UNII:DIF093I037)	AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY	5 [hp_X]  in 300 mg
NITRIC ACID (UNII: 411VRN1TV4) (NITRIC ACID - UNII:411VRN1TV4)	NITRIC ACID	6 [hp_X]  in 300 mg
KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E)	KEROSENE	6 [hp_X]  in 300 mg

Inactive Ingredients
Ingredient Name	Strength
LACTOSE (UNII: J2B2A4N98G)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	white	Score	no score
Shape	ROUND (Tablet)	Size	9mm
Flavor		Imprint Code	Heel
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50114-6134-2	30000 mg in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		01/31/1984

Labeler - Heel Inc (102783016)

Establishment
Name	Address	ID/FEI	Business Operations
Heel Inc		102783016	manufacture