GUNA ALLERGY

Manufacturer
Guna spa
Effective date
2020-10-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:13:26

Label at a glance#

ProductGUNA ALLERGY
Active ingredientHISTAMINE DIHYDROCHLORIDE, SUS SCROFA ADRENAL GLAND, EPINEPHRINE, APIS MELLIFERA, CUPRIC ACETATE, SILVER NITRATE, DRIMIA MARITIMA BULB, GALPHIMIA GLAUCA FLOWERING TOP, SCHOENOCAULON OFFICINALE SEED, SODIUM CHLORIDE, LUFFA OPERCULATA FRUIT, MATRICARIA CHAMOMILLA WHOLE, AMMONIUM CARBONATE, ONION, ARSENIC TRIOXIDE, SUS SCROFA NASAL MUCOSA
Label structure10 sections

Dosage and administration

Take 15 minutes before meals. Adults and children 12 years and older: 20 drops in a little water 2 times per day Children between 12 years and 6 years of age :10 drops in a little water 2 times per day Children under 6 years: consult a physician

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS/PURPOSE

OTC - ACTIVE INGREDIENT SECTION

CHAMOMILLA 3X RELIEVES INFLAMMATION

GLANDULA SUPRARENALIS SUIS 6X 12X 30X SUPPORTS METABOLISM

MUCOSA NASALIS SUIS 200X RELIEVES ALLERGY SYMPTOMS

SCILLA MARITIMA 12X 30X 200X RELIEVES DRY COUGH

SABADILLA 12X 30X 200X RELIEVES HAY FEVER

ALLIUM CEPA 12X 30X 200X RELIEVES RESPIRATORY CONGESTION

AMMONIUM CARBONICUM 12X 30X 200X RELIEVES RESPIRATORY CONGESTION

APIS MELLIFICA 200X HELPS REDUCE SWELLING

ARGENTUM NITRICUM 30X RELIEVES INFLAMMATION

ARSENICUM ALBUM 12X 30X 200X RELIEVES INFLAMMATION

CUPRUM ACETICUM 12X 30X 200X RELIEVES HAY FEVER, PERSISTENT COUGH

GALPHIMIA GLAUCA 6X 12X 200X RELIEVES HAY FEVER

LUFFA OPERCULATA 6X 12X 30X RELIEVES HAY FEVER

HISTAMINUM HYDROCHLORICUM 200X RELIEVES ALLERGY SYMPTOMS

NATRUM MURIATICUM 12X 30X 200X RELIEVES ALLERGY SYMPTOMS

ADRENALINUM 6X IMMUNE SUPPORT

WARNINGS

WARNINGS SECTION

  • Stop use and ask doctor if symptoms persist more than 5 days.
  • If pregnant or breast-feeding ask a health care professional before use.
  • Keep out of reach of children.
  • In case of accidental overdose, seek professional assistance or contact a poison control center immediately.
  • Contains ethyl alcohol 30%

WARNINGS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children


DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Take 15 minutes before meals.

Adults and children 12 years and older: 20 drops in a little water 2 times per day


Children between 12 years and 6 years of age :10 drops in a little water 2 times per day


Children under 6 years: consult a physician



QUESTIONS

OTC - QUESTIONS SECTION

Questions?: info@gunainc.com, tel. (484) 223-3500

INDICATIONS & USAGE SECTION

Take 15 minutes before meals.

INACTIVE INGREDIENT SECTION

Inactive ingredient: Ethyl alcohol 30%.

PURPOSE

OTC - PURPOSE SECTION

TEMPORARILY RELIEVES SYMPTOMS OF SEASONAL ALLERGIES SUCH AS:

  • SNEEZING
  • NASAL DISCHARGE
  • ITCHY, WATERY EYES

OTC - DO NOT USE SECTION

DO NOT USE

If tamper-evident seal is broken

stop use and ask doctor if symptoms persist more than 5 days

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5USALL5USALL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-461-18GUNA ALLERGY1 in 1 BOXSOLUTION/ DROPS12
17089-461-18GUNA ALLERGY30 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-461GUNA ALLERGY (ADRENALINUM - ALLIUM CEPA - AMMONIUM CARBONICUM - APIS MELLIFICA - ARGENTUM NITRICUM - ARSENICUM ALBUM - CUPRUM ACETICUM - GALPHIMIA GLAUCA - GLANDULA SUPRARENALIS SUIS - HISTAMINUM HYDROCHLORICUM - LUFFA OPERCULATA - MATRICARIA CHAMOMILLA - MUCOSA NASALIS SUIS - NATRUM MURIATICUM - SABADILLA - SCILLA MARITIMA -) SOLUTION/ DROPS [GUNA SPA]2Current NDC, Legacy NDC, 2 package rows20201024_ae6bd80d-2c70-1a3f-e053-2a95a90a2652.zip

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17089-46117089-461-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 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
GUNA ALLERGYADRENALINUM - ALLIUM CEPA - AMMONIUM CARBONICUM - APIS MELLIFICA - ARGENTUM NITRICUM - ARSENICUM ALBUM - CUPRUM ACETICUM - GALPHIMIA GLAUCA - GLANDULA SUPRARENALIS SUIS - HISTAMINUM HYDROCHLORICUM - LUFFA OPERCULATA - MATRICARIA CHAMOMILLA - MUCOSA NASALIS SUIS - NATRUM MURIATICUM - SABADILLA - SCILLA MARITIMA -Guna spaae6bd80d-2c70-1a3f-e053-2a95a90a26522020-10-23WarningsExact identifier
ndc (package): 17089-461-18
ndc (product): 17089-461
ndc11 (package): 17089046118
spl id: b2580118-8598-5057-e053-2a95a90aab4e
spl set id: ae6bd80d-2c70-1a3f-e053-2a95a90a2652

Reported adverse events (FAERS/openFDA)#

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