Indications and uses
For the temporary relief of symptoms due to Seasonal Allergies such as: Sneezing, Watery Eyes, Runny nose
For the temporary relief of symptoms due to Seasonal Allergies such as: Sneezing, Watery Eyes, Runny nose
Adults and children 12 years and older 2 sprays to each nostril , 3-5 times per day Children between 12 years and 6 years of age 1 spray to each nostril, 3-5 times per day Children under 6 years 1 spray to each nostril, 3 times per day
ALIUM CEPA 6X, 8X, 12X EXPECTORANT
APIS MELLIFICA 12x, 30X, 200X DECONGESTANT
ARALIA RACEMOSA 1X ANTITUSSIVE
ARGENTUM NITRICUM 10X ANALGESIC
ASCORBIC ACID 2X ANTIOXIDANT
BLACK CURRANT, BARK 1X DETOXIFICATION
CISTUS CANADENSIS 4X HELPS BRONCHIAL SECRETION
CUPRUM METALLICUM 4X ANTIOXIDANT
EUPHORBIUM OFFICINARUM 4X MUCOLYTIC
HISTAMINUM HYDROCHLORICUM 30X, 200X ANTI-INFLAMMATORY
INTERFERON GAMMA 4C ANTIVIRAL
INTERLEUKIN 10 4C ANTI-INFLAMMATORY
INTERLEUKIN 12 4C SUPPORTS IMMUNE ACTIVITY
MANGANESE GLUCONATE 4X DECONGESTANT
MELILOTUS OFFICINALIS 3X DECONGESTANT
PLANTAGO MAJOR 2X DETOXIFICATION
ROSA CANINA, BARK 1X PAIN RELIEF
SAMBUCUS NIGRA 2X ANTITUSSIVE
For the temporary relief of symptoms due to Seasonal Allergies such as: Sneezing, Watery Eyes, Runny nose
Stop use and ask doctor if symptoms worsen or persist more than 5 days
If pregnant or breast-feeding ask a doctor before use
Keep this and all medicines out of reach of children
Adults and children 12 years and older 2 sprays to each nostril , 3-5 times per day
Children between 12 years and 6 years of age 1 spray to each nostril, 3-5 times per day
Children under 6 years 1 spray to each nostril, 3 times per day
Questions?: info@gunainc.com
Tel. (484) 223-3500
Tilt head slightly forward, place tip of bottle into nose, compress bottle once for each spray, aiming towards the back of the nose.
Inactive ingredients: Water, Orange juice, Potassium sorbate, Sodium benzoate
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| c599c4a0-705d-4ebb-ab1f-977af038f96a | Product name | 1 | 20251124 |
| 503ea967-4b9c-48cf-9e87-c7975295849d | Product name | 2 | 20220120 |
| c5cd4727-ac49-4409-82b1-5bd8006c3ec7 | Product name | 1 | 20171122 |
| d45267e3-883a-4760-85b5-ebc565c21683 | Product name | 1 | 20150910 |
| 6cca4355-1206-91f7-02de-17eef38a8622 | Product name | 1 | 20140508 |
| 751c581a-bf64-2fd7-b3ec-ca02c83e4a00 | Product name | 1 | 20140508 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17089-419-23 | GUNA-RHINO NOSE | 30 mL in 1 BOTTLE, SPRAY | SPRAY | 30 | 2 | |
| 17089-419-23 | GUNA-RHINO NOSE | 1 in 1 BOX | SPRAY | 1 | 2 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 17089-419 | GUNA-RHINO NOSE (APIS MELLIFERA - ARALIA RACEMOSA ROOT - ASCORBIC ACID - BLACK CURRANT - COPPER - EUPHORBIA RESINIFERA RESIN - EUROPEAN ELDERBERRY - HELIANTHEMUM CANADENSE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - HUMAN INTERLEUKIN-10 (NONGLYCOSYLATED) - INTERFERON GAMMA-1B - MANGANESE GLUCONATE - MELILOTUS - ONION - PLANTAGO MAJOR - ROSA CANINA FRUIT - SILVER NITRATE -) SPRAY [GUNA SPA] | 2 | Current NDC, Legacy NDC, 2 package rows | 20190406_5baeb698-1735-4586-9984-2a2cb0da871a.zip |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| APIS MELLIFERA | ACTIVE INGREDIENT | 7S82P3R43Z | 1 | |
| ARALIA RACEMOSA ROOT | ACTIVE INGREDIENT | T90W4582DU | 1 | |
| ASCORBIC ACID | ACTIVE INGREDIENT | PQ6CK8PD0R | 1 | |
| BLACK CURRANT | ACTIVE INGREDIENT | 9755T40D11 | 1 | |
| COPPER | ACTIVE INGREDIENT | 789U1901C5 | 1 | |
| EUPHORBIA RESINIFERA RESIN | ACTIVE INGREDIENT | 1TI1O9028K | 1 | |
| EUROPEAN ELDERBERRY | ACTIVE INGREDIENT | BQY1UBX046 | 1 | |
| HELIANTHEMUM CANADENSE | ACTIVE INGREDIENT | 46G3W789Q3 | 1 | |
| HISTAMINE DIHYDROCHLORIDE | ACTIVE INGREDIENT | 3POA0Q644U | 1 | |
| HUMAN INTERLEUKIN 12 | ACTIVE INGREDIENT | 7B590791ER | 1 | |
| HUMAN INTERLEUKIN-10 (NONGLYCOSYLATED) | ACTIVE INGREDIENT | 9SC4O216V9 | 1 | |
| INTERFERON GAMMA-1B | ACTIVE INGREDIENT | 21K6M2I7AG | 1 | |
| MANGANESE GLUCONATE | ACTIVE INGREDIENT | 9YY2F980SV | 1 | |
| MELILOTUS | ACTIVE INGREDIENT | F22I9R6Q0X | 1 | |
| ONION | ACTIVE INGREDIENT | 492225Q21H | 1 | |
| PLANTAGO MAJOR | ACTIVE INGREDIENT | W2469WNO6U | 1 | |
| ROSA CANINA FRUIT | ACTIVE INGREDIENT | 3TNW8D08V3 | 1 | |
| SILVER NITRATE | ACTIVE INGREDIENT | 95IT3W8JZE | 1 | |
| APIS MELLIFERA | ACTIVE MOIETY | 7S82P3R43Z | 1 | |
| ARALIA RACEMOSA ROOT | ACTIVE MOIETY | T90W4582DU | 1 | |
| ASCORBIC ACID | ACTIVE MOIETY | PQ6CK8PD0R | 1 | |
| BLACK CURRANT | ACTIVE MOIETY | 9755T40D11 | 1 | |
| COPPER | ACTIVE MOIETY | 789U1901C5 | 1 | |
| EUPHORBIA RESINIFERA RESIN | ACTIVE MOIETY | 1TI1O9028K | 1 | |
| EUROPEAN ELDERBERRY | ACTIVE MOIETY | BQY1UBX046 | 1 | |
| HELIANTHEMUM CANADENSE | ACTIVE MOIETY | 46G3W789Q3 | 1 | |
| HISTAMINE | ACTIVE MOIETY | 820484N8I3 | 1 | |
| HUMAN INTERLEUKIN 12 | ACTIVE MOIETY | 7B590791ER | 1 | |
| HUMAN INTERLEUKIN-10 (NONGLYCOSYLATED) | ACTIVE MOIETY | 9SC4O216V9 | 1 | |
| INTERFERON GAMMA-1B | ACTIVE MOIETY | 21K6M2I7AG | 1 | |
| MANGANESE CATION (2+) | ACTIVE MOIETY | H6EP7W5457 | 1 | |
| MELILOTUS | ACTIVE MOIETY | F22I9R6Q0X | 1 | |
| ONION | ACTIVE MOIETY | 492225Q21H | 1 | |
| PLANTAGO MAJOR | ACTIVE MOIETY | W2469WNO6U | 1 | |
| ROSA CANINA FRUIT | ACTIVE MOIETY | 3TNW8D08V3 | 1 | |
| SILVER CATION | ACTIVE MOIETY | 57N7B0K90A | 1 | |
| ORANGE JUICE | INACTIVE INGREDIENT | 5A9KE2L9L3 | 1 | |
| POTASSIUM SORBATE | INACTIVE INGREDIENT | 1VPU26JZZ4 | 1 | |
| SODIUM BENZOATE | INACTIVE INGREDIENT | OJ245FE5EU | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 17089-419 | 17089-419-23 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ORANGE JUICE | 5A9KE2L9L3 | IACT |
| POTASSIUM SORBATE | 1VPU26JZZ4 | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
| ONION | 492225Q21H | ACTIB |
| APIS MELLIFERA | 7S82P3R43Z | ACTIB |
| ARALIA RACEMOSA ROOT | T90W4582DU | ACTIB |
| SILVER NITRATE | 95IT3W8JZE | ACTIB |
| ASCORBIC ACID | PQ6CK8PD0R | ACTIB |
| BLACK CURRANT | 9755T40D11 | ACTIB |
| HELIANTHEMUM CANADENSE | 46G3W789Q3 | ACTIB |
| COPPER | 789U1901C5 | ACTIB |
| EUPHORBIA RESINIFERA RESIN | 1TI1O9028K | ACTIB |
| HISTAMINE DIHYDROCHLORIDE | 3POA0Q644U | ACTIB |
| INTERFERON GAMMA-1B | 21K6M2I7AG | ACTIB |
| INTERLEUKIN-10 | 9SC4O216V9 | ACTIB |
| HUMAN INTERLEUKIN 12 | 7B590791ER | ACTIB |
| MANGANESE GLUCONATE | 9YY2F980SV | ACTIB |
| MELILOTUS | F22I9R6Q0X | ACTIB |
| PLANTAGO MAJOR | W2469WNO6U | ACTIB |
| ROSA CANINA FRUIT | 3TNW8D08V3 | ACTIB |
| EUROPEAN ELDERBERRY | BQY1UBX046 | ACTIB |
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | TABLET, FILM COATED / ORAL | 1 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SUSPENSION / ORAL | 320 mg | ||
| ORANGE JUICE | ORANGE JUICE | 5A9KE2L9L3 | SOLUTION / ORAL | NA | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | TABLET, FILM COATED / ORAL | 1 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | TABLET, COATED / ORAL | 0.2 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | CAPSULE / ORAL | 8.5 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | ELIXIR / ORAL | 5.02 mg/5ml | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | POWDER, FOR SOLUTION / ORAL | 98 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SYRUP / ORAL | 80 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | PASTE / ORAL | 48 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | GRANULE / ORAL | NA | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | GRANULE, FOR SUSPENSION / ORAL | 120 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | TABLET, COATED / ORAL | 0.2 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | POWDER, FOR SUSPENSION / ORAL | 19 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | TABLET, EXTENDED RELEASE / ORAL | 0.2 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | CAPSULE / ORAL | NA | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | POWDER, FOR SUSPENSION / ORAL | 160 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | TABLET, COATED / ORAL | NA | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | SYRUP / ORAL | 2 mg/1ml | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | POWDER, FOR SOLUTION / ORAL | 98 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | POWDER, FOR SUSPENSION / ORAL | 160 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | CAPSULE / ORAL | 8.5 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | PASTE / ORAL | 48 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | TABLET, EXTENDED RELEASE / ORAL | NA | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | SOLUTION / ORAL | 1000 mg/15ml | ||
| ORANGE JUICE | ORANGE JUICE | 5A9KE2L9L3 | SOLUTION / ORAL | NA | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | GRANULE, FOR SUSPENSION / ORAL | 80 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SUSPENSION/ DROPS / ORAL | 23 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | SUSPENSION / ORAL | 400 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SUSPENSION, EXTENDED RELEASE / ORAL | 24 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | TABLET / ORAL | 30 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | GRANULE, FOR SUSPENSION / ORAL | 120 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | TABLET, FILM COATED, EXTENDED RELEASE / ORAL | 0.2 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | CONCENTRATE / ORAL | 1 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | PASTE / ORAL | 28 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | SUSPENSION / ORAL | 400 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | TABLET, FILM COATED, EXTENDED RELEASE / ORAL | 0.2 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | PASTE / ORAL | 28 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | CONCENTRATE / ORAL | 1 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | SYRUP / ORAL | 2 mg/1ml | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | TABLET, EXTENDED RELEASE / ORAL | 0.2 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SYRUP / ORAL | 80 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | TABLET / ORAL | 6 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | GRANULE, EFFERVESCENT / ORAL | 60 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | POWDER, FOR SUSPENSION / ORAL | 19 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SUSPENSION/ DROPS / ORAL | 23 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SUSPENSION, EXTENDED RELEASE / ORAL | 24 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | TABLET, DELAYED RELEASE / ORAL | 0.34 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | ELIXIR / ORAL | 5.02 mg/5ml | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | CONCENTRATE / ORAL | 20 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | TABLET, EXTENDED RELEASE / ORAL | NA | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | TABLET, DELAYED RELEASE / ORAL | 0.34 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SOLUTION / ORAL | 660 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | CAPSULE / ORAL | NA | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SOLUTION / ORAL | 660 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | TABLET / ORAL | 6 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SUSPENSION / ORAL | 320 mg | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | GRANULE, FOR SUSPENSION / ORAL | 80 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | GRANULE / ORAL | NA | ||
| POTASSIUM SORBATE | POTASSIUM SORBATE | 1VPU26JZZ4 | TABLET, COATED / ORAL | NA |
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 |
|---|---|---|---|---|---|---|
| GUNA-RHINO NOSE | APIS MELLIFERA - ARALIA RACEMOSA ROOT - ASCORBIC ACID - BLACK CURRANT - COPPER - EUPHORBIA RESINIFERA RESIN - EUROPEAN ELDERBERRY - HELIANTHEMUM CANADENSE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - HUMAN INTERLEUKIN-10 (NONGLYCOSYLATED) - INTERFERON GAMMA-1B - MANGANESE GLUCONATE - MELILOTUS - ONION - PLANTAGO MAJOR - ROSA CANINA FRUIT - SILVER NITRATE - | Guna spa | 5baeb698-1735-4586-9984-2a2cb0da871a | 2018-12-21 | Warnings | 17089-419-23 17089-419 17089041923 7e02aa23-f955-6990-e053-2a91aa0af032 5baeb698-1735-4586-9984-2a2cb0da871a |
Adverse event summaries are temporarily unavailable. Other product information remains available.