FDA.reportPublic FDA data

GUNA-ALLERGY T

Manufacturer
Guna spa
Effective date
2026-06-10
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
daily-update
Hydrated at
2026-06-12 05:10:09

Label at a glance#

ProductGUNA-ALLERGY T
Active ingredientEPINEPHRINE, ONION, AMMONIUM CARBONATE, APIS MELLIFERA, ARSENIC TRIOXIDE, BLATTA ORIENTALIS, SUS SCROFA BRONCHUS, CUPRIC ACETATE, GALPHIMIA GLAUCA FLOWERING TOP, SUS SCROFA ADRENAL GLAND, HISTAMINE DIHYDROCHLORIDE, LUFFA OPERCULATA FRUIT, MANGANESE GLUCONATE, SUS SCROFA NASAL MUCOSA, SODIUM CHLORIDE, SCHOENOCAULON OFFICINALE SEED, DRIMIA MARITIMA BULB
Label structure10 sections

Indications and uses

Temporary relief of symptoms due to seasonal allergies such as: Sneezing Runny nose Itchy eyes Watery eyes

Dosage and administration

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

ADRENALINUM 6X IMMUNE STRENGTHENING

ALIUM CEPA 12X 30X 200X DECONGESTANT

AMMONIUM CARBONICUM 12X 30X 200X DECONGESTANT

APIS MELLIFICA 200X ANTI-INFLAMMATORY

ARSENICUM ALBUM 12X 30X 200X IMMUNE SUPPORT

BLATTA ORIENTALIS 6X 12X 30X DETOXIFICATION

BRONCHUS 200X RESPIRATORY TRACT SUPPORT

CUPRUM ACETICUM 12X 30X 200X METABOLIC SUPPORT

GALPHIMIA GLAUCA 6X 12X 30X ALLERGY SYMPTOM RELIEF

GLANDULA SUPRARENALIS 6X 12X 30X HORMONAL SUPPORT

HISTAMINUM HYDROCHLORICUM 200X DETOXIFICATION

LUFFA OPERCULATA 6X 12X 30X DETOXIFICATION

MANGANESE GLUCONATE 4X METABOLIC SUPPORT

MUCOSA NASALIS 200X RESPIRATORY SYSTEM SUPPORT

NATRUM MURIATICUM 12X 30X 200X IMMUNE SUPPORT

SABADILLA 12X 30X 200X DETOXIFICATION

SCILLA MARITIMA 12X 30X 200X ALLERGY SYMPTOM RELIEF

USES

OTC - PURPOSE SECTION

Temporary relief of symptoms due to seasonal allergies such as:

  • Sneezing
  • Runny nose
  • Itchy eyes
  • Watery eyes

WARNINGS

WARNINGS SECTION

  • Stop use and ask doctor if symptoms persist more than 5 days.
  • If pregnant or breast-feeding ask a health professional before use.
  • Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
  • Contains ethyl alcohol 30%

PREGNANCY

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding ask a doctor before use

WARNINGS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children


DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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%.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5USTRE-Guna-Allergy-T-Rev04-05-07-20245USTRE-Guna-Allergy-T-Rev04-05-07-2024

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData Matrix5USTRE5USTRE-Guna-Allergy-T-Rev04-05-07-2024.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0b4ec9ca-d305-43fc-88dd-7a510313efe0Product name120260105
bb209f42-a85f-4fee-9d3d-c9dded168625Product name120251208
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419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
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c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17089-418-182020-03-13C16284748780-19d75b9cf-f0d7-f424-e053-dadaa90a57ceGUNA-ALLERGY T
17089-418-182020-03-13C16284748780-19d75b9cf-f0d7-f424-e053-dadaa90a57ceGUNA-ALLERGY T
17089-418-182020-01-31C16284748780-19d75b9cf-f0d7-f424-e053-dadaa90a57ceGUNA-ALLERGY T
17089-418-182020-01-31C16284748780-19d75b9cf-f0d7-f424-e053-dadaa90a57ceGUNA-ALLERGY T

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AMMONIUM CARBONATEACTIVE INGREDIENTNJ5VT0FKLJ1
APIS MELLIFERAACTIVE INGREDIENT7S82P3R43Z1
ARSENIC TRIOXIDEACTIVE INGREDIENTS7V92P67HO1
BLATTA ORIENTALISACTIVE INGREDIENT535787266D1
CUPRIC ACETATEACTIVE INGREDIENT39M11XPH031
DRIMIA MARITIMA BULBACTIVE INGREDIENT3629601H5D1
EPINEPHRINEACTIVE INGREDIENTYKH834O4BH1
GALPHIMIA GLAUCA FLOWERING TOPACTIVE INGREDIENT93PH5Q8M7E1
HISTAMINE DIHYDROCHLORIDEACTIVE INGREDIENT3POA0Q644U1
LUFFA OPERCULATA FRUITACTIVE INGREDIENTC4MO6809HU1
MANGANESE GLUCONATEACTIVE INGREDIENT9YY2F980SV1
ONIONACTIVE INGREDIENT492225Q21H1
SCHOENOCAULON OFFICINALE SEEDACTIVE INGREDIENT6NAF1689IO1
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8X1
SUS SCROFA ADRENAL GLANDACTIVE INGREDIENT398IYQ16YV1
SUS SCROFA BRONCHUSACTIVE INGREDIENTK34664156J1
SUS SCROFA NASAL MUCOSAACTIVE INGREDIENTID3Z1X61WY1
AMMONIAACTIVE MOIETY5138Q19F1X1
APIS MELLIFERAACTIVE MOIETY7S82P3R43Z1
ARSENIC TRIOXIDEACTIVE MOIETYS7V92P67HO1
BLATTA ORIENTALISACTIVE MOIETY535787266D1
CHLORIDE IONACTIVE MOIETYQ32ZN486981
CUPRIC CATIONACTIVE MOIETY8CBV67279L1
DRIMIA MARITIMA BULBACTIVE MOIETY3629601H5D1
EPINEPHRINEACTIVE MOIETYYKH834O4BH1
GALPHIMIA GLAUCA FLOWERING TOPACTIVE MOIETY93PH5Q8M7E1
HISTAMINEACTIVE MOIETY820484N8I31
LUFFA OPERCULATA FRUITACTIVE MOIETYC4MO6809HU1
MANGANESE CATION (2+)ACTIVE MOIETYH6EP7W54571
ONIONACTIVE MOIETY492225Q21H1
SCHOENOCAULON OFFICINALE SEEDACTIVE MOIETY6NAF1689IO1
SUS SCROFA ADRENAL GLANDACTIVE MOIETY398IYQ16YV1
SUS SCROFA BRONCHUSACTIVE MOIETYK34664156J1
SUS SCROFA NASAL MUCOSAACTIVE MOIETYID3Z1X61WY1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17089-41817089-418-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
EPINEPHRINEYKH834O4BHACTIB
ONION492225Q21HACTIB
AMMONIUM CARBONATENJ5VT0FKLJACTIB
APIS MELLIFERA7S82P3R43ZACTIB
ARSENIC TRIOXIDES7V92P67HOACTIB
BLATTA ORIENTALIS535787266DACTIB
SUS SCROFA BRONCHUSK34664156JACTIB
CUPRIC ACETATE39M11XPH03ACTIB
GALPHIMIA GLAUCA FLOWERING TOP93PH5Q8M7EACTIB
SUS SCROFA ADRENAL GLAND398IYQ16YVACTIB
HISTAMINE DIHYDROCHLORIDE3POA0Q644UACTIB
LUFFA OPERCULATA FRUITC4MO6809HUACTIB
MANGANESE GLUCONATE9YY2F980SVACTIB
SUS SCROFA NASAL MUCOSAID3Z1X61WYACTIB
SODIUM CHLORIDE451W47IQ8XACTIB
SCHOENOCAULON OFFICINALE SEED6NAF1689IOACTIB
DRIMIA MARITIMA BULB3629601H5DACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52022-11-15full-release2026-06-01 02:18:34

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 22 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii+route
22 equally ranked IID candidates

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-ALLERGY TAMMONIUM CARBONATE - APIS MELLIFERA - ARSENIC TRIOXIDE - BLATTA ORIENTALIS - CUPRIC ACETATE - DRIMIA MARITIMA BULB - EPINEPHRINE - GALPHIMIA GLAUCA FLOWERING TOP - HISTAMINE DIHYDROCHLORIDE - LUFFA OPERCULATA - MANGANESE GLUCONATE - ONION - SCHOENOCAULON OFFICINALE SEED - SODIUM CHLORIDE - SUS SCROFA ADRENAL GLAND - SUS SCROFA BRONCHUS - SUS SCROFA NASAL MUCOSA -Guna spafddba85e-2bec-468f-a01a-b71a3aeed9d32026-06-10WarningsExact identifier
ndc (package): 17089-418-18
ndc (product): 17089-418
ndc11 (package): 17089041818
spl id: 53ea3900-f754-760c-e063-6294a90af2d2
spl set id: fddba85e-2bec-468f-a01a-b71a3aeed9d3

Reported adverse events (FAERS/openFDA)#

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