United States · FDA National Drug Code directory
SunDrops 75
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
- 63621-356_435330fc-c021-151b-e063-6394a90a229b
- Product NDC
- 63621-356
- Form
- GEL
- Composition / generic term
- Alcohol
- Labeler
- Sunburst Chemicals, Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20091014
- Source listing expiry
- 20261231
Source-listed ingredients
- ALCOHOL — .6 mL/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 3785 mL in 1 BOTTLE, PLASTIC (63621-356-14) · 63621-356-14
- 8 BAG in 1 BOX (63621-356-20) / 1000 mL in 1 BAG · 63621-356-20
- 12 BOTTLE, PUMP in 1 BOX (63621-356-25) / 236.6 mL in 1 BOTTLE, PUMP · 63621-356-25
- 4 BAG in 1 BOX (63621-356-40) / 1000 mL in 1 BAG · 63621-356-40
- 473.2 mL in 1 BOTTLE, PUMP (63621-356-50) · 63621-356-50
Source and coverage
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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.
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