FDA.reportPublic FDA data

GUNA HAY FEVER RELIEF

Manufacturer
Guna spa
Effective date
2021-12-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:15:13

Label at a glance#

ProductGUNA HAY FEVER RELIEF
Active ingredientSTRYCHNOS NUX-VOMICA SEED, HISTAMINE DIHYDROCHLORIDE, MANGANESE, SCHOENOCAULON OFFICINALE SEED, ONION, APIS MELLIFERA, SILVER NITRATE, EUPHRASIA STRICTA, GALPHIMIA GLAUCA FLOWERING TOP, SULFUR, ARSENIC TRIOXIDE
Label structure13 sections

Indications and uses

Temporarily relieves hay fever symptoms, such as: ● sneezing ● coughing ● inflamed, runny nose

Dosage and administration

Turn tube upside down and rotate cap to release pellets into cap. ● Unscrew cap and, without touching the pellets, place them under the tongue. ● Allow to dissolve. ● Take 15 minutes before meals.

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Temporarily relieves hay fever symptoms, such as:

● sneezing

● coughing

● inflamed, runny nose

QUESTIONS

OTC - QUESTIONS SECTION

Questions?

info@gunainc.com



(484) 223-3500

WARNINGS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

PREGNANCY

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

USES

OTC - PURPOSE SECTION

Temporarily relieves hay fever symptoms, such as:

● sneezing

● coughing

● inflamed, runny nose

WARNINGS

OTC - STOP USE SECTION

  • Stop use and ask doctor if symptoms persist more than 5 days or worsen.
  • If pregnant or breast-feeding ask a health care professional before use
  • keep out of reach of children

WARNINGS SECTION

  • Stop use and ask doctor if symptoms persist more than 5 days or worsen.
  • If pregnant or breast-feeding ask a health professional before use.
  • Do not use more than the recommended dose.
  • Keep out of reach of children.

ACTIVE INGREDIENTS/PURPOSE

OTC - ACTIVE INGREDIENT SECTION

Allium cepa 30X Relieves sneezing, runny nose

Apis mellifica 200X Helps reduce swelling

Galphimia glauca 4X Relieves sneezing, coughing, blocked nose

Argentum nitricum 6X Relieves sneezing, runny nose

Arsenicum album 30X Relieves allergy symptoms

Euphrasia officinalis 5X Relieves inflamed nose and eye mucosa

Histaminum hydrochloricum 200X Relieves allergy symptoms

Manganum metallicum 8X Relieves hoarseness

Nux vomica 4X Relieves sneezing, coughing, blocked nose

Sabadilla 6X Relieves sneezing, coughing, blocked nose

Sulphur 30X Relieves inflamed nose and eye mucosa

DIRECTIONS

OTC - WHEN USING SECTION

  • Turn tube upside down and rotate cap to release pellets into cap. ● Unscrew cap and, without touching the pellets, place them under the tongue. ● Allow to dissolve. ● Take 15 minutes before meals.

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 12 years and older 5 pellets 3 times per day
  • Children between 12 and 6 years of age 3 pellets 3 times per day
  • Children under 6 years 1 pellet 3 times per day to be disoolved into a little water

INACTIVE INGREDIENT SECTION

Inactive ingredient: Sucrose.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5USHFR-65USHFR-65USHF1 B5USHF1 B

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-476-20GUNA HAY FEVER RELIEF4 g in 1 TUBEPELLET43
17089-476-20GUNA HAY FEVER RELIEF2 in 1 BOXPELLET23
17089-476-21GUNA HAY FEVER RELIEF4 g in 1 TUBEPELLET43
17089-476-21GUNA HAY FEVER RELIEF1 in 1 BOXPELLET13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-476GUNA HAY FEVER RELIEF (STRYCHNOS NUX VOMICA SEED - HISTAMINE DIHYDROCHLORIDE - MANGANESE - SCHOENOCAULON OFFICINALE SEED - APIS MELLIFERA - ARSENIC TRIOXIDE - SILVER NITRATE - ONION - EUPHRASIA STRICTA - GALPHIMIA GLAUCA FLOWERING TOP - SULFUR -) PELLET [GUNA SPA]3Current NDC, Legacy NDC, 4 package rows20211216_b8db4fc6-f235-6f2b-e053-2a95a90a186f.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17089-47617089-476-20, 17089-476-21

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
HISTAMINE DIHYDROCHLORIDE3POA0Q644UACTIB
MANGANESE42Z2K6ZL8PACTIB
SCHOENOCAULON OFFICINALE SEED6NAF1689IOACTIB
ONION492225Q21HACTIB
SUCROSEC151H8M554IACT
APIS MELLIFERA7S82P3R43ZACTIB
SILVER NITRATE95IT3W8JZEACTIB
EUPHRASIA STRICTAC9642I91WLACTIB
GALPHIMIA GLAUCA FLOWERING TOP93PH5Q8M7EACTIB
SULFUR70FD1KFU70ACTIB
ARSENIC TRIOXIDES7V92P67HOACTIB

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
GUNA HAY FEVER RELIEFSTRYCHNOS NUX VOMICA SEED - HISTAMINE DIHYDROCHLORIDE - MANGANESE - SCHOENOCAULON OFFICINALE SEED - APIS MELLIFERA - ARSENIC TRIOXIDE - SILVER NITRATE - ONION - EUPHRASIA STRICTA - GALPHIMIA GLAUCA FLOWERING TOP - SULFUR -Guna spab8db4fc6-f235-6f2b-e053-2a95a90a186f2021-12-15WarningsExact identifier
ndc (package): 17089-476-21
ndc (package): 17089-476-20
ndc (product): 17089-476
ndc11 (package): 17089047620
ndc11 (package): 17089047621
spl id: d3322d60-dd44-8e96-e053-2995a90a54b0
spl set id: b8db4fc6-f235-6f2b-e053-2a95a90a186f

Reported adverse events (FAERS/openFDA)#

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