Home NDC 87765-001 CELISTAR MICRONEEDLING INFUSION
Product NDC 87765-001
11-digit product format 877650001
Labeler code 87765
Product ID 87765-001_53de2aff-a7e1-23fc-e063-6294a90a7731
Type HUMAN OTC DRUG
Nonproprietary name HYALURONATE SODIUM
Dosage form LIQUID
Route TOPICAL
Labeler Guangdong Outeli Biotechnology Co., Ltd.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-10
Substance HYALURONATE SODIUM; HYDROLYSED MARINE COLLAGEN (ENZYMATIC; 2000 MW)
Active strength 3.5; 2.5 g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base CELISTAR MICRONEEDLING INFUSION
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HYALURONATE SODIUM 3.5 g/100mL HYDROLYSED MARINE COLLAGEN (ENZYMATIC 2.5 g/100mL 2000 MW)
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination YSE9PPT4TH Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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.
Matched openFDA labels page 30 of 68 · 1,357 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87765-001-01 87765000101 20 mL in 1 BOX (87765-001-01) 20 ml 2026-06-10 No No Current 87765-001-02 87765000102 10 mL in 1 BOX (87765-001-02) 10 ml 2026-06-10 No No Current