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#
Contacts and useful links#
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
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0220-0219-41 | 2023-10-18 | C162847 | 48780-1 | f386c649-eb71-0266-e053-dadaa90a7c1a | Ambrosia artemisiaefolia 30C |
| 0220-0219-43 | 2023-10-18 | C162847 | 48780-1 | f386c649-eb71-0266-e053-dadaa90a7c1a | Ambrosia artemisiaefolia 30C |
| 0220-0219-41 | 2023-01-30 | C162847 | 48780-1 | f386c649-eb71-0266-e053-dadaa90a7c1a | Ambrosia artemisiaefolia 30C |
| 0220-0219-43 | 2023-01-30 | C162847 | 48780-1 | f386c649-eb71-0266-e053-dadaa90a7c1a | Ambrosia artemisiaefolia 30C |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0220-0219-41 | Ambrosia artemisiaefolia | 30 [hp_C] in 1 TUBE | PELLET | 30 | 8 | |
| 0220-0219-43 | Ambrosia artemisiaefolia | 3 in 1 PACKAGE | PELLET | 3 | 8 | |
| 0220-0219-43 | Ambrosia artemisiaefolia | 30 [hp_C] in 1 TUBE | PELLET | 30 | 8 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Ambrosia artemisiaefolia
- AMBROSIA ARTEMISIIFOLIA
- LACTOSE, UNSPECIFIED FORM
- ANHYDROUS LACTOSE
- SUCROSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0220-0219 | 0220-0219-41, 0220-0219-43 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| LACTOSE, UNSPECIFIED FORM | J2B2A4N98G | IACT |
| SUCROSE | C151H8M554 | IACT |
| AMBROSIA ARTEMISIIFOLIA | 9W34L2CQ9A | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Ambrosia artemisiaefolia | AMBROSIA ARTEMISIIFOLIA | Boiron | 8427717f-4d1a-54b5-e053-2a91aa0a3d00 | 2024-02-08 | 0220-0219-41 0220-0219-43 0220-0219 00220021941 00220021943 10e04d03-329d-090f-e063-6294a90a6c72 8427717f-4d1a-54b5-e053-2a91aa0a3d00 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.




