BHI ACNE- silver nitrate, arnica montana, atropa belladonna, bryonia alba root, solanum dulcamara top, echinacea purpurea, calcium sulfide, lachesis muta venom, phytolacca americana root, pulsatilla vulgaris, rancid beef, toxicodendron pubescens leaf, and thuja occidentalis leafy twig tablet

BHI Acne by

Drug Labeling and Warnings

BHI Acne by is a Homeopathic medication manufactured, distributed, or labeled by MediNatura. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Each tablet contains: Argentum nitricum 8X,*Arnica montana, radix 6X, *Belladonna 4X, *Bryonia alba 5X, *Dulcamara 6X, *Echinacea purpurea 2X, Hepar sulphuris calcareum 10X, *Lachesis mutus 12X, *Phytolacca decandra 6X, *Pulsatilla 6X, *Pyrogenium 12X, *Rhus toxicodendron 6X, *Thuja occidentalis 6X 23.1 mg each.

*Natural Ingredients

INACTIVE INGREDIENTS

Lactose, Magnesium stearate

USES

Uses: For the temporary relief of minor acne symptoms: redness, pain, and tenderness

WARNINGS

Warnings: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted. Do not use if known sensitivity to Acne or any of its ingredients exists.

Tamper Evident: Use this product only if imprinted shrink seal around neck and cap is intact.

KEEP OUT OF REACH OF CHILDREN

keep out of reach of children

DIRECTIONS

Directions: At first sign of symptoms: Adults and children 12 years and older:1 tablet every 1/2 to 1 hour until symptoms lessen, then continue with standard dosage. Do not exceed 12 tablets in 24 hours.

Standard dosage: Adults and children 12 years and older: 3 tablets per day, taking 1 tablet every 4 to 6 hours.

For children under 12, consult your health professional.

Allow tablets to dissolve completely in the mouth, do not swallow.

USES

Acne Relief Tablets

Relieves:

Redness

Pain

Tenderness

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BHI ACNE 
silver nitrate, arnica montana, atropa belladonna, bryonia alba root, solanum dulcamara top, echinacea purpurea, calcium sulfide, lachesis muta venom, phytolacca americana root, pulsatilla vulgaris, rancid beef, toxicodendron pubescens leaf, and thuja occidentalis leafy twig tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62795-1013
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A)	SILVER NITRATE	8 [hp_X]
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	8 [hp_X]
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H)	ATROPA BELLADONNA	4 [hp_X]
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B)	BRYONIA ALBA ROOT	5 [hp_X]
SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N)	SOLANUM DULCAMARA TOP	6 [hp_X]
ECHINACEA PURPUREA (UNII: QI7G114Y98) (ECHINACEA PURPUREA - UNII:QI7G114Y98)	ECHINACEA PURPUREA	2 [hp_X]
CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q)	CALCIUM SULFIDE	10 [hp_X]
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	12 [hp_X]
PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG)	PHYTOLACCA AMERICANA ROOT	6 [hp_X]
PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV)	PULSATILLA VULGARIS	6 [hp_X]
RANCID BEEF (UNII: 29SUH5R3HU) (RANCID BEEF - UNII:29SUH5R3HU)	RANCID BEEF	12 [hp_X]
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A)	TOXICODENDRON PUBESCENS LEAF	6 [hp_X]
THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397)	THUJA OCCIDENTALIS LEAFY TWIG	6 [hp_X]

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

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code	Leafman
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62795-1013-2	100 in 1 BOTTLE; Type 0: Not a Combination Product	09/30/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/30/2014

Labeler - MediNatura (079324099)

Establishment
Name	Address	ID/FEI	Business Operations
MediNatura		102783016	manufacture(62795-1013)