OTC - ACTIVE INGREDIENT SECTION
Sulfate, Potassium Ion, Chloride Ion
Rurina
- Manufacturer
- NANO BIO TECH CO.,Ltd
- Effective date
- 2018-01-01
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-05-31 22:53:55
Label at a glance#
ProductRurina
Active ingredientSULFATE ION, POTASSIUM CATION, CHLORIDE ION
Label structure8 sections
Label contents#
Full prescribing information#
INACTIVE INGREDIENT SECTION
Al, Ca, Ga, La, Li, Mn, Nd, Si, Zn
OTC - PURPOSE SECTION
First aid to help prevent infection in minor:
- cuts
- scrapes
- burns
WARNINGS SECTION
Do not use
- if you are allergic to any of the ingredients
- in the eyes
- over large areas of the body
Ask a doctor before use if you have
- deep or puncture wounds
- animal bites
- serious burns
Stop use and ask a doctor if
- you need to use longer than 1 week
- condition persists or gets worse
- rash or other allergic reaction develops
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
INDICATIONS & USAGE SECTION
Apply to the area which is wounded or burnt
DOSAGE & ADMINISTRATION SECTION
for external use only
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 71608-0001-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-1e8d-f424-e053-dadaa90a57ce | 55e6ea26-a898-2791-e054-00144ff8d46c |
Products#
Every source-derived product name is available through these pages.
- Rurina
- Sulfate, Potassium Ion, Chloride Ion
- MAGNESIUM
- SULFATE ION
- POTASSIUM CATION
- CHLORIDE ION
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 71608-0001 | 71608-0001-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MAGNESIUM | I38ZP9992A | IACT |
| SULFATE ION | 7IS9N8KPMG | ACTIB |
| POTASSIUM CATION | 295O53K152 | ACTIB |
| CHLORIDE ION | Q32ZN48698 | ACTIB |
Source Document#
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 |
|---|---|---|---|---|---|---|
| 61c3305e-a45a-1ad9-e053-2a91aa0a6b63 | 55e6ea26-a898-2791-e054-00144ff8d46c | 2018-01-01 | Warnings | 61c3305e-a45a-1ad9-e053-2a91aa0a6b63 55e6ea26-a898-2791-e054-00144ff8d46c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.