Everyday Sunscreen SPF 50

Product NDC

75936-135

11-digit product format

759360135

Labeler code

75936

Product ID

75936-135_3bb571a8-4e7c-4431-ab8e-f797560be9f6

Type

HUMAN OTC DRUG

Nonproprietary name

Avobenzone, Homosalate, Octinoxate, Octisalate

Dosage form

LOTION

Route

TOPICAL

Labeler

TAYLOR JAMES, LTD.

Application

part352

Marketing category

OTC MONOGRAPH FINAL

Marketing start

2015-01-20

Marketing end

0000-00-00

Substance

AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE

Active strength

3 g/100mL; g/100mL; g/100mL; g/100mL

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record