Lubriderm Daily Moisture

Product NDC

58232-0753

11-digit product format

582320753

Labeler code

58232

Product ID

58232-0753_fc2d9e39-b4e1-4ff0-a3b5-2c35ff07d8f2

Type

HUMAN OTC DRUG

Nonproprietary name

Avobenzone, Octisalate, Octocrylene, and Oxybenzone

Dosage form

LOTION

Route

TOPICAL

Labeler

Johnson & Johnson Consumer Inc.

Application

part352

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2010-07-01

Marketing end

2019-08-01

Substance

AVOBENZONE; OCTISALATE; OCTOCRYLENE; OXYBENZONE

Active strength

20 mg/mL; mg/mL; mg/mL; mg/mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record