NDC 68229-601 – SunBurnt PLUS

Lidocaine Hydrochloride 4 g/100mL · Gel · Topical

Human Otc Drug

Product NDC68229-601

Product details

Brand name
SunBurnt PLUS
Generic name
Lidocaine Hydrochloride
Labeler
Quest Products, LLC.
Dosage form
Gel
Route
Topical
Marketing category
OTC MONOGRAPH DRUG · M017
Marketed since
February 23, 2024
Listing expires
December 31, 2026
Pharmacologic class
Amide Local Anesthetic; Antiarrhythmic

Active ingredients

Uses, dosage, side effects and warnings for SunBurnt PLUS →

Package NDC codes (1)

Package NDCDescriptionSince
68229-601-021 TUBE in 1 CARTON (68229-601-02) / 118 mL in 1 TUBE (68229-601-01)Feb 23, 2024