Indications and uses
CHRONIC VIRAL INFECTIONS
GUNA-INF GAMMA
- Manufacturer
- Guna spa
- Effective date
- 2022-11-15
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 5
- Source
- full-release
- Hydrated at
- 2026-06-01 02:18:33
Label at a glance#
ProductGUNA-INF GAMMA
Active ingredientINTERFERON GAMMA-1B
Label structure10 sections
Dosage and administration
Take 15 minutes before meals. Adults and children 12 years and older 20 drops twice a day in a little water. Hold in the mouth for about 30 seconds then swallow. Children between 12 years and 6 years of age 10 drops twice a day in a little water. Hold in the mouth for about 30 seconds then swallow. Children under 6 years 5 drops twice a day in a glass of water.
Contacts and useful links#
Label contents#
Full prescribing information#
ACTIVE INGREDIENTS/PURPOSE
INTERFERON GAMMA-1B 4C CHRONIC VIRAL INFECTIONS
USES
CHRONIC VIRAL INFECTIONS
WARNINGS
Stop use and ask doctor if symptoms worsen or persist more than 5 days
PREGNANCY
If pregnant or breast-feeding ask a doctor before use
WARNINGS
Keep this and all medicines out of reach of children
DIRECTIONS
Take 15 minutes before meals.
Adults and children 12 years and older 20 drops twice a day in a little water. Hold in the mouth for about 30 seconds then swallow.
Children between 12 years and 6 years of age 10 drops twice a day in a little water. Hold in the mouth for about 30 seconds then swallow.
Children under 6 years 5 drops twice a day in a glass of water.
QUESTIONS
Questions?: info@gunainc.com
Tel. (484) 223-3500
INACTIVE INGREDIENT SECTION
INACTIVE INGREDIENT: ETHYL ALCOHOL 30%.
INDICATIONS & USAGE SECTION
Take 15 minutes before meals.
PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| d45267e3-883a-4760-85b5-ebc565c21683 | Product name | 1 | 20150910 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 17089-378-18 | 2020-03-13 | C162847 | 48780-1 | 9d75b9d1-23d3-f424-e053-dadaa90a57ce | GUNA-INF GAMMA |
| 17089-378-18 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-23d3-f424-e053-dadaa90a57ce | GUNA-INF GAMMA |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17089-378-18 | GUNA-INF GAMMA | 30 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 30 | 5 | |
| 17089-378-18 | GUNA-INF GAMMA | 1 in 1 BOX | SOLUTION/ DROPS | 1 | 5 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| INTERFERON GAMMA-1B | ACTIVE INGREDIENT | 21K6M2I7AG | 1 | |
| INTERFERON GAMMA-1B | ACTIVE MOIETY | 21K6M2I7AG | 1 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 1 |
Products#
Every source-derived product name is available through these pages.
- GUNA-INF GAMMA
- INTERFERON GAMMA-1B
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 17089-378 | 17089-378-18 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | IACT |
| INTERFERON GAMMA-1B | 21K6M2I7AG | ACTIB |
Source Document#
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg |
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-INF GAMMA | INTERFERON GAMMA-1B | Guna spa | a09a33a1-5c7c-493d-abc7-907edd8e97ca | 2022-11-15 | Warnings | 17089-378-18 17089-378 17089037818 ed813de7-e0d5-74b9-e053-2995a90a6a73 a09a33a1-5c7c-493d-abc7-907edd8e97ca |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.