GUNA-SINUS NOSE
- Product NDC
- 17089-451
- 11-digit product format
- 170890451
- Labeler code
- 17089
- Product ID
- 17089-451_7d9d997a-fda9-2a63-e053-2a91aa0a0000
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALTHAEA OFFICINALIS LEAF - ASCORBIC ACID - BLACK CURRANT - CALCIUM SULFIDE - COPPER - ECHINACEA ANGUSTIFOLIA - GOLDENSEAL - LACHESIS MUTA VENOM - LOBARIA PULMONARIA - MANGANESE - MERCURIC SULFIDE - ONION - PLANTAGO MAJOR - POTASSIUM CARBONATE - PULSATILLA VULGARIS - SILICON DIOXIDE - SILVER NITRATE - SINUSITISINUM - SUS SCROFA NASAL MUCOSA - SUS SCROFA THYMUS - SUS SCROFA URINARY BLADDER -
- Dosage form
- SPRAY
- Route
- NASAL
- Labeler
- Guna spa
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2010-05-27
- Substance
- ALTHAEA OFFICINALIS LEAF; ASCORBIC ACID; BLACK CURRANT; CALCIUM SULFIDE; COPPER; ECHINACEA ANGUSTIFOLIA; GOLDENSEAL; LACHESIS MUTA VENOM; LOBARIA PULMONARIA; MANGANESE; MERCURIC SULFIDE; ONION; PLANTAGO MAJOR; POTASSIUM DICHROMATE; PULSATILLA VULGARIS; SILICON DIOXIDE; SILVER NITRATE; SINUSITISINUM; SUS SCROFA NASAL MUCOSA; SUS SCROFA THYMUS; SUS SCROFA URINARY BLADDER
- Active strength
- 2; 2; 1; 8; 3; 3; 8; 30; 2; 3; 8; 8; 2; 8; 8; 8; 10; 30; 12; 12; 30 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
- Pharmacologic classes
- Allergens [CS], Ascorbic Acid [CS], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Inhibit Ovum Fertilization [PE], Non-Standardized Food Allergenic Extract [EPC], Vegetable Proteins [CS], Vitamin C [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- GUNA-SINUS NOSE
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ONION | 2 [hp_X]/30mL |
| ALTHAEA OFFICINALIS LEAF | 2 [hp_X]/30mL |
| SILVER NITRATE | 1 [hp_X]/30mL |
| ASCORBIC ACID | 8 [hp_X]/30mL |
| BLACK CURRANT | 3 [hp_X]/30mL |
| LOBARIA PULMONARIA | 3 [hp_X]/30mL |
| COPPER | 8 [hp_X]/30mL |
| ECHINACEA ANGUSTIFOLIA | 30 [hp_X]/30mL |
| CALCIUM SULFIDE | 2 [hp_X]/30mL |
| GOLDENSEAL | 3 [hp_X]/30mL |
| POTASSIUM DICHROMATE | 8 [hp_X]/30mL |
| LACHESIS MUTA VENOM | 8 [hp_X]/30mL |
| MANGANESE | 2 [hp_X]/30mL |
| MERCURIC SULFIDE | 8 [hp_X]/30mL |
| SUS SCROFA NASAL MUCOSA | 8 [hp_X]/30mL |
| PLANTAGO MAJOR | 8 [hp_X]/30mL |
| PULSATILLA VULGARIS | 10 [hp_X]/30mL |
| SILICON DIOXIDE | 30 [hp_X]/30mL |
| SINUSITISINUM | 12 [hp_X]/30mL |
| SUS SCROFA THYMUS | 12 [hp_X]/30mL |
| SUS SCROFA URINARY BLADDER | 30 [hp_X]/30mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 492225Q21H | Internal UNII lookup |
| E2QQV92338 | Internal UNII lookup |
| 95IT3W8JZE | Internal UNII lookup |
| PQ6CK8PD0R | Internal UNII lookup |
| 9755T40D11 | Internal UNII lookup |
| D1YM0P5Z2T | Internal UNII lookup |
| 789U1901C5 | Internal UNII lookup |
| VB06AV5US8 | Internal UNII lookup |
| 1MBW07J51Q | Internal UNII lookup |
| ZW3Z11D0JV | Internal UNII lookup |
| T4423S18FM | Internal UNII lookup |
| VSW71SS07I | Internal UNII lookup |
| 42Z2K6ZL8P | Internal UNII lookup |
| ZI0T668SF1 | Internal UNII lookup |
| ID3Z1X61WY | Internal UNII lookup |
| W2469WNO6U | Internal UNII lookup |
| I76KB35JEV | Internal UNII lookup |
| ETJ7Z6XBU4 | Internal UNII lookup |
| B575563DM5 | Internal UNII lookup |
| 7B69B0BD62 | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 36fef678-17c6-4d2a-a0f0-ddb298611f25 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| c599c4a0-705d-4ebb-ab1f-977af038f96a | Product name | 1 | 20251124 |
| c5cd4727-ac49-4409-82b1-5bd8006c3ec7 | Product name | 1 | 20171122 |
| 6cca4355-1206-91f7-02de-17eef38a8622 | Product name | 1 | 20140508 |
| 751c581a-bf64-2fd7-b3ec-ca02c83e4a00 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17089-451-23 | GUNA-SINUS NOSE | 30 mL in 1 BOTTLE, SPRAY | SPRAY | 30 | 3 | |
| 17089-451-23 | GUNA-SINUS NOSE | 1 in 1 BOX | SPRAY | 1 | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 17089-451 | GUNA-SINUS NOSE (ALTHAEA OFFICINALIS LEAF - ASCORBIC ACID - BLACK CURRANT - CALCIUM SULFIDE - COPPER - ECHINACEA ANGUSTIFOLIA - GOLDENSEAL - LACHESIS MUTA VENOM - LOBARIA PULMONARIA - MANGANESE - MERCURIC SULFIDE - ONION - PLANTAGO MAJOR - POTASSIUM CARBONATE - PULSATILLA VULGARIS - SILICON DIOXIDE - SILVER NITRATE - SINUSITISINUM - SUS SCROFA NASAL MUCOSA - SUS SCROFA THYMUS - SUS SCROFA URINARY BLADDER -) SPRAY [GUNA SPA] | 3 | Current NDC, Legacy NDC, 2 package rows | 20190404_36fef678-17c6-4d2a-a0f0-ddb298611f25.zip |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| GUNA-SINUS NOSE | ALTHAEA OFFICINALIS LEAF - ASCORBIC ACID - BLACK CURRANT - CALCIUM SULFIDE - COPPER - ECHINACEA ANGUSTIFOLIA - GOLDENSEAL - LACHESIS MUTA VENOM - LOBARIA PULMONARIA - MANGANESE - MERCURIC SULFIDE - ONION - PLANTAGO MAJOR - POTASSIUM CARBONATE - PULSATILLA VULGARIS - SILICON DIOXIDE - SILVER NITRATE - SINUSITISINUM - SUS SCROFA NASAL MUCOSA - SUS SCROFA THYMUS - SUS SCROFA URINARY BLADDER - | Guna spa | 36fef678-17c6-4d2a-a0f0-ddb298611f25 | 2018-12-22 | Warnings | 17089-451 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 17089-451-23 | 17089045123 | 1 BOTTLE, SPRAY in 1 BOX (17089-451-23) / 30 mL in 1 BOTTLE, SPRAY | 2018-12-21 | 0000-00-00 | No | No | Current |