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.

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Ambrosia artemisiaefolia 30C

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:

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 TypeHUMAN OTC DRUGItem Code (Source)NDC:0220-0219
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (AMBROSIA ARTEMISIIFOLIA - UNII:9W34L2CQ9A) AMBROSIA ARTEMISIIFOLIA30 [hp_C]  in 30 [hp_C]
Inactive Ingredients
Ingredient NameStrength
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
SUCROSE (UNII: C151H8M554)  
Product Characteristics
ColorwhiteScore    
ShapeROUNDSize4mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0220-0219-4130 [hp_C] in 1 TUBE; Type 0: Not a Combination Product03/03/1983
2NDC:0220-0219-433 in 1 PACKAGE05/11/2020
230 [hp_C] in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic03/03/1983
Labeler - Boiron (282560473)
Registrant - Boiron, Inc. (014892269)
Establishment
NameAddressID/FEIBusiness Operations
Boiron282560473manufacture(0220-0219)

Revised: 2/2024
Document Id: 10e04d03-329d-090f-e063-6294a90a6c72
Set id: 8427717f-4d1a-54b5-e053-2a91aa0a3d00
Version: 8
Effective Time: 20240208
 
Boiron