Kiehls Since 1851 CrossTerrain UV Skin Protector

Product NDC

49967-382

11-digit product format

499670382

Labeler code

49967

Product ID

49967-382_db4d13f8-fd4b-4642-b4a9-13c889b63c34

Type

HUMAN OTC DRUG

Nonproprietary name

Avobenzone Homosalate Octisalate Octocrylene Oxybenzone

Dosage form

OINTMENT

Route

TOPICAL

Labeler

L'Oreal USA Products Inc

Application

part352

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2010-06-01

Marketing end

0000-00-00

Substance

AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE

Active strength

1 g/40g; g/40g; g/40g; g/40g; g/40g

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record