warnings
Do not use on broken, irritated, or sensitive skin. Avoid contact with eyes. lf contact occurs,rinse immediately with plenty of water. Discontinue use immediately if discomfort or irritation occurs.
CELISTAR MICRONEEDLING INFUSION
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- CELISTAR MICRONEEDLING INFUSION
- Generic name
- HYALURONATE SODIUM
- Manufacturer
- Guangdong Outeli Biotechnology Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 53de46a7-3947-70a7-e063-6294a90ab829
- SPL ID
- 53de2aff-a7e1-23fc-e063-6294a90a7731
- Version
- 1
- Effective date
- 2026-06-09
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:20:09
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M016 | openfda.application_number | |
| brand name | CELISTAR MICRONEEDLING INFUSION | openfda.brand_name | |
| generic name | HYALURONATE SODIUM | openfda.generic_name | |
| manufacturer name | Guangdong Outeli Biotechnology Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 87765-001-02 | openfda.package_ndc |
| ndc | package | 87765-001-01 | openfda.package_ndc |
| ndc | product | 87765-001 | openfda.product_ndc |
| ndc11 | package | 87765000102 | derived:openfda.package_ndc |
| ndc11 | package | 87765000101 | derived:openfda.package_ndc |
| spl id | 53de2aff-a7e1-23fc-e063-6294a90a7731 | id | |
| spl set id | 53de46a7-3947-70a7-e063-6294a90ab829 | set_id | |
| unii | YSE9PPT4TH | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.