Ambrosia artemisiaefolia

Manufacturer
Boiron | Boiron, Inc.
Effective date
2024-02-08
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 02:26:01

Label at a glance#

ProductAmbrosia artemisiaefolia
Active ingredientAMBROSIA ARTEMISIIFOLIA
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

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.

OTC - PURPOSE SECTION

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

INDICATIONS & USAGE SECTION

Box Purpose*

Relieves symptoms of hay fever associated with ragweed allergy

Tube Purpose

Relieves symptoms of hay fever*

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

SPL UNCLASSIFIED SECTION

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.

INACTIVE INGREDIENT SECTION

lactose, sucrose

DOSAGE & ADMINISTRATION SECTION

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.

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0219-41Ambrosia artemisiaefolia30 [hp_C] in 1 TUBEPELLET308
0220-0219-43Ambrosia artemisiaefolia3 in 1 PACKAGEPELLET38
0220-0219-43Ambrosia artemisiaefolia30 [hp_C] in 1 TUBEPELLET308

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0219AMBROSIA ARTEMISIAEFOLIA (AMBROSIA ARTEMISIIFOLIA ) PELLET [BOIRON]8Current NDC, Legacy NDC, 3 package rows20240209_8427717f-4d1a-54b5-e053-2a91aa0a3d00.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-02190220-0219-41, 0220-0219-43

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ambrosia artemisiaefoliaAMBROSIA ARTEMISIIFOLIABoiron8427717f-4d1a-54b5-e053-2a91aa0a3d002024-02-08Exact identifier
ndc (package): 0220-0219-41
ndc (package): 0220-0219-43
ndc (product): 0220-0219
ndc11 (package): 00220021941
ndc11 (package): 00220021943
spl id: 10e04d03-329d-090f-e063-6294a90a6c72
spl set id: 8427717f-4d1a-54b5-e053-2a91aa0a3d00

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.