United States · FDA National Drug Code directory
SunDrops 87
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 63621-387_435389b8-9dde-0d17-e063-6294a90ab9b8
- Product NDC
- 63621-387
- Form
- SOAP
- Composition / generic term
- Benzalkonium Chloride
- Labeler
- Sunburst Chemicals, Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20200608
- Source listing expiry
- 20261231
Source-listed ingredients
- BENZALKONIUM CHLORIDE — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 4 BAG in 1 BOX (63621-387-40) / 1000 mL in 1 BAG · 63621-387-40
- 6 BOTTLE, PUMP in 1 BOX (63621-387-50) / 500 mL in 1 BOTTLE, PUMP · 63621-387-50
- 8 BAG in 1 BOX (63621-387-65) / 1000 mL in 1 BAG · 63621-387-65
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →