fine finish pressed powder W21

Product NDC

71220-016

11-digit product format

712200016

Labeler code

71220

Product ID

71220-016_b8f6c2b5-68b3-442b-b3d3-bd8d99a88252

Type

HUMAN OTC DRUG

Nonproprietary name

OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE

Dosage form

LOTION

Route

TOPICAL

Labeler

Innisfree Corporation

Application

part352

Marketing category

OTC MONOGRAPH FINAL

Marketing start

2017-06-23

Marketing end

0000-00-00

Substance

OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE

Active strength

3 g/13g; g/13g; g/13g

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record