ACONITUM NAPELLUS pellet

Aconitum napellus by

Drug Labeling and Warnings

Aconitum napellus by is a Homeopathic medication manufactured, distributed, or labeled by Laboratoires Boiron, Boiron Inc., Boiron. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Aconitum napellus HPUS
3X, 6X, 12X, 30X, 6C, 9C, 12C, 15C, 30C, 200CK, 1M, 10M, 50M

PURPOSE

Use

High fever (up to 102f) of sudden onset with dry skin*

Warnings

Stop use and ask a doctor if

symptoms persist for more than 3 days or worsen.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

Directions

5 pellets 3 times a day until symptoms are relieved.

Other information

Do not use if pellet dispenser seal is broken.
contains approx. 80 pellets

Inactive ingredients

lactose, sucrose

Questions, Comments?

1-800-BOIRON-1
Newtown Square, PA 19073-3267
info@boironusa.com

*

These "Uses" have not been evaluated by the FDA.

Principle Display Panel - Aconitum napellus HPUS 3X

Principle Display Panel - Aconitum napellus HPUS 6X

Principle Display Panel - Aconitum napellus HPUS 12X

Principle Display Panel - Aconitum napellus HPUS 30X

Principle Display Panel - Aconitum napellus HPUS 6C

Principle Display Panel - Aconitum napellus HPUS 9C

Principle Display Panel - Aconitum napellus HPUS 12C

Principle Display Panel - Aconitum napellus HPUS 15C

Principle Display Panel - Aconitum napellus HPUS 30C

Principle Display Panel - Aconitum napellus HPUS 200CK

Principle Display Panel - Aconitum napellus HPUS 1M

Principle Display Panel - Aconitum napellus HPUS 10M

Principle Display Panel - Aconitum napellus HPUS 50M

INGREDIENTS AND APPEARANCE

ACONITUM NAPELLUS 
aconitum napellus pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0220-0050
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD)	ACONITUM NAPELLUS	3 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
SUCROSE (UNII: C151H8M554)
LACTOSE (UNII: J2B2A4N98G)

Product Characteristics
Color	white	Score
Shape	ROUND	Size	4mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0220-0050-41	80 in 1 TUBE; Type 0: Not a Combination Product	03/03/1983

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		03/03/1983

Labeler - Laboratoires Boiron (282560473)

Registrant - Boiron Inc. (014892269)

Establishment
Name	Address	ID/FEI	Business Operations
Boiron		282560473	manufacture(0220-0050)

Establishment
Name	Address	ID/FEI	Business Operations
Boiron		380022322	manufacture(0220-0050)