Dr.Jart Every Sun Day Sunscreen SPF 50

Product NDC

49404-130

11-digit product format

494040130

Labeler code

49404

Product ID

49404-130_3f42326a-6b16-31eb-e054-00144ff88e88

Type

HUMAN OTC DRUG

Nonproprietary name

ZINC OXIDE, OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE

Dosage form

CREAM

Route

TOPICAL

Labeler

Have & Be Co., Ltd.

Application

part352

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2016-01-25

Marketing end

0000-00-00

Substance

ZINC OXIDE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE

Active strength

6 mg/50mL; mg/50mL; mg/50mL; mg/50mL

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record