Indications and uses
TEMPORARY PAIN RELIEF
GUNA-IL 10
- Manufacturer
- Guna spa
- Effective date
- 2026-06-10
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 6
- Source
- daily-update
- Hydrated at
- 2026-06-12 05:10:08
Label at a glance#
ProductGUNA-IL 10
Active ingredientINTERLEUKIN-10
Label structure10 sections
Dosage and administration
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 consult a physician
Contacts and useful links#
Label contents#
Full prescribing information#
ACTIVE INGREDIENTS/PURPOSE
INTERLEUKIN-10 4C TEMPORARY PAIN RELIEF
USES
TEMPORARY PAIN RELIEF
WARNINGS
Stop use and ask doctor if symptoms worsen or persist more than 5 days.
If pregnant or breast-feeding ask a doctor professional before use.
Keep this and all medicines out of reach of children.
Contains ethyl alcohol 30%
PREGNANCY
If pregnant or breast-feeding ask a doctor before use.
WARNINGS
Keep this and all medicines out of reach of children.
DIRECTIONS
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 consult a physician
QUESTIONS
Questions?: info@gunainc.com
Tel. (484) 223-3500
INDICATIONS & USAGE SECTION
Directions: Take 15 minutes before meals.
INACTIVE INGREDIENT SECTION
Inactive ingredient: Ethyl alcohol 30%.
PRINCIPAL DISPLAY PANEL
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Data code | Data Matrix | 5U1I10 | 5U1I10-Rev05.jpg |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 17089-388-18 | 2020-03-13 | C162847 | 48780-1 | 9d75b9cf-e906-f424-e053-dadaa90a57ce | GUNA-IL 10 |
| 17089-388-18 | 2020-03-13 | C162847 | 48780-1 | 9d75b9cf-e906-f424-e053-dadaa90a57ce | GUNA-IL 10 |
| 17089-388-18 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-e906-f424-e053-dadaa90a57ce | GUNA-IL 10 |
| 17089-388-18 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-e906-f424-e053-dadaa90a57ce | GUNA-IL 10 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| INTERLEUKIN-10 | ACTIVE INGREDIENT | 9SC4O216V9 | 1 | |
| INTERLEUKIN-10 | ACTIVE MOIETY | 9SC4O216V9 | 1 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 1 |
Products#
Every source-derived product name is available through these pages.
- GUNA-IL 10
- INTERLEUKIN-10
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 17089-388 | 17089-388-18 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | IACT |
| INTERLEUKIN-10 | 9SC4O216V9 | ACTIB |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 5 | 2022-11-15 | full-release | 2026-06-01 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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml |
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-IL 10 | INTERLEUKIN-10 | Guna spa | d6faade4-6263-44d3-b278-12088eb56e46 | 2026-06-10 | Warnings | 17089-388-18 17089-388 17089038818 53e9f2bb-21fd-d6c8-e063-6294a90ae615 d6faade4-6263-44d3-b278-12088eb56e46 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.