88118-001-01 5 mL Sterile Saline Solution
- Manufacturer
- BIOLOGIX USA, INC.
- Effective date
- 2026-10-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- daily-update
- Hydrated at
- 2026-11-03 06:04:56
Label at a glance#
Label contents#
Full prescribing information#
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
keep out of reach of children
INDICATIONS & USAGE SECTION
This product is designed for gentle cleaning of the face, mouth, nose, eyes, ears, and wounds. It can also be used with a nebulizer to help relieve discomfort in the nose and mouth.
WARNINGS SECTION
warnings
DOSAGE & ADMINISTRATION SECTION
Single-Use Ampules 5 mL each
OTC - ACTIVE INGREDIENT SECTION
active ingredient
INACTIVE INGREDIENT SECTION
inactive ingredients
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
package label
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0860016515611 | GTIN-13: 0860016515611 EAN-13: 0860016515611 GTIN-12: 860016515611 UPC-A: 860016515611 GTIN storage (14 digits): 00860016515611 | 4.jpg |
Products#
Every source-derived product name is available through these pages.
- BiologixCare Sterile Saline Wound Wash
- Sodium Chloride
- CHLORIDE ION
- SODIUM CATION
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 88118-001 | 88118-001-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM CHLORIDE | 451W47IQ8X | ACTIB |
| WATER | 059QF0KO0R | IACT |
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 |
|---|---|---|---|---|---|---|
| BiologixCare Sterile Saline Wound Wash | SODIUM CHLORIDE | BIOLOGIX USA, INC. | 5edb1f1e-122d-f0da-e063-6394a90a4ccd | 2026-10-29 | Warnings | 88118-001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.





