SkinTx UV Pro Broad Spectrum SPF30

Product NDC

42521-2930

11-digit product format

425212930

Labeler code

42521

Product ID

42521-2930_96b3a99e-d624-48c4-a63e-586130cfceb9

Type

HUMAN OTC DRUG

Nonproprietary name

ZINC OXIDE, OCTINOXATE, OCTISALATE

Dosage form

LOTION

Route

TOPICAL

Labeler

Dermolab Pharma Ltd

Application

part352

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2015-05-14

Marketing end

0000-00-00

Substance

ZINC OXIDE; OCTINOXATE; OCTISALATE

Active strength

99 mg/mL; mg/mL; mg/mL

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record