Ambrosia Artemisiaefolia: Homeopathic Product Information

AMBROSIA ARTEMISIAEFOLIA- ambrosia artemisiifolia pellet
Boiron

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.

Active ingredients**

Ambrosia artemisiaefolia 30C HPUS (0.44 mg)

The letters “HPUS” indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

Uses*

temporarily relieves one or more of these symptoms of hay fever associated with ragweed allergy including:

  • runny nose
  • irritated eyes
  • sneezing
  • itchy throat and nose

Box Purpose*

Relieves symptoms of hay fever associated with ragweed allergy

Tube Purpose

Relieves symptoms of hay fever*

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. In case of accidental overdose, get medical help or contact a Poison Control Center right away.

Ragweed Allergy Relief*

On-the-Go Allergy Relief*

Non-Drowsy

3 Tubes

Approx. 80 Pellets Each

Total 240 Pellets

16 Doses per tube

do not use if glued carton end flaps are open or if pellet dispenser seal is broken

contains 0.25 g of sugar per dose

retain carton for full drug facts

How to dispense pellets? Turn tube upside down. Twist until 5 pellets are dispensed into cap. Carefully remove the cap and use it to pour pellets under the tongue.
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
*C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

lactose, sucrose

Directions

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

1-800-BOIRON-1 (1-800-264-7661),
BoironUSA.com Info@boiron.com
Distributed by Boiron, Inc. Newtown Square, PA 19073

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AMBROSIA ARTEMISIAEFOLIA
ambrosia artemisiifolia pellet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0220-0219
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AMBROSIA ARTEMISIIFOLIA (AMBROSIA ARTEMISIIFOLIA) AMBROSIA ARTEMISIIFOLIA 30 [hp_C] in 30 [hp_C]
Inactive Ingredients
Ingredient Name Strength
LACTOSE, UNSPECIFIED FORM (ANHYDROUS LACTOSE)
SUCROSE
Product Characteristics
Color white Score
Shape ROUND Size 4mm
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0220-0219-41 30 [hp_C] in 1 TUBE None
2 NDC:0220-0219-43 3 TUBE in 1 PACKAGE contains a TUBE
2 30 [hp_C] in 1 TUBE This package is contained within the PACKAGE (0220-0219-43)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 03/03/1983
Labeler — Boiron (282560473)
Registrant — Boiron, Inc. (014892269)
Establishment
Name Address ID/FEI Operations
Boiron 282560473 manufacture (0220-0219)

Revised: 02/2024 Boiron

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