LOreal Paris Sublime Sun

Product NDC

49967-229

11-digit product format

499670229

Labeler code

49967

Product ID

49967-229_7a672eef-693f-4bf0-8df1-6fc782187540

Type

HUMAN OTC DRUG

Nonproprietary name

Avobenzone Homosalate Octisalate Octocrylene Oxybenzone

Dosage form

LOTION

Route

TOPICAL

Labeler

L'Oreal USA Products Inc

Application

part352

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2011-10-01

Marketing end

0000-00-00

Substance

AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE

Active strength

3 mL/88mL; mL/88mL; mL/88mL; mL/88mL; mL/88mL

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record