NDC 63621-356 – SunDrops 75

Alcohol .6 mL/mL · Gel · Topical

Human Otc Drug

Product NDC63621-356

Product details

Brand name
SunDrops 75
Generic name
Alcohol
Labeler
Sunburst Chemicals, Inc.
Dosage form
Gel
Route
Topical
Marketing category
OTC MONOGRAPH DRUG · 505G(a)(3)
Marketed since
October 14, 2009
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for SunDrops 75 →

Package NDC codes (5)

Package NDCDescriptionSince
63621-356-143785 mL in 1 BOTTLE, PLASTIC (63621-356-14)May 7, 2020
63621-356-208 BAG in 1 BOX (63621-356-20) / 1000 mL in 1 BAGOct 14, 2009
63621-356-2512 BOTTLE, PUMP in 1 BOX (63621-356-25) / 236.6 mL in 1 BOTTLE, PUMPOct 14, 2009
63621-356-404 BAG in 1 BOX (63621-356-40) / 1000 mL in 1 BAGOct 16, 2025
63621-356-50473.2 mL in 1 BOTTLE, PUMP (63621-356-50)Jun 29, 2020