Galphimia glauca

Manufacturer
Boiron | Boiron, Inc.
Effective date
2023-02-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:20:19

Label at a glance#

ProductGalphimia glauca
Active ingredientGALPHIMIA GLAUCA FLOWERING TOP
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient** (in each pellet)

Galphimia glauca 30C HPUS (0.44 mg)

OTC - PURPOSE SECTION

Purpose*

Relieves hay fever symptoms

INDICATIONS & USAGE SECTION

Uses*

Box - temporarily relieves symptoms of hay fever (allergic rhinitis) caused by seasonal pollens, dust mites, mold, or pet dander and saliva such as:

  • itchy, stuffy, or runny nose
  • nasal congestion
  • eye irritation

Tube- Itchy Nose And Sneezing Due To 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 breastfeeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

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.

SPL UNCLASSIFIED SECTION

Box-

  • 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

Hay Fever Relief*

Itchy or Runny Nose Sneezing Watery Eyes*

Turn the tube upside down

Twist until 5 pellets are dispensed

Remove cap and pour pellets under the tongue

3 Tubes

Approx. 80 Pellets Each

Total 240 Pellets

16 Doses per tube

Seasonal Pollens & Indoor Allergies*

Non-Drowsy

Tube-

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

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

labellabellabellabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-2241-41Galphimia glauca30 [hp_C] in 1 TUBEPELLET303
0220-2241-43Galphimia glauca30 [hp_C] in 1 TUBEPELLET303
0220-2241-43Galphimia glauca3 in 1 BOXPELLET33

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-2241GALPHIMIA GLAUCA (GALPHIMIA GLAUCA FLOWERING TOP ) PELLET [BOIRON]3Current NDC, Legacy NDC, 3 package rows20230223_85a20448-494b-8363-e053-2a91aa0a0473.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
0220-22410220-2241-41, 0220-2241-43

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
Galphimia glaucaGALPHIMIA GLAUCA FLOWERING TOPBoiron85a20448-494b-8363-e053-2a91aa0a04732023-02-20Exact identifier
ndc (package): 0220-2241-43
ndc (package): 0220-2241-41
ndc (product): 0220-2241
ndc11 (package): 00220224141
ndc11 (package): 00220224143
spl id: f52c2b0f-8c93-8e55-e053-2995a90a8299
spl set id: 85a20448-494b-8363-e053-2a91aa0a0473

Reported adverse events (FAERS/openFDA)#

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