FACEBLOCK- titanium dioxide and zinc oxide lotion

FACEBLOCK by

Drug Labeling and Warnings

FACEBLOCK by is a Otc medication manufactured, distributed, or labeled by Gordon Laboratories, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

active ingredients

Titanium Dioxide (6.7%), Zinc Oxide (9.2%).

other ingredients

Water (Aqua), Cyclopentasiloxane, Dimethicone, Butylene Glycol, Dicaprylyl Ether, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Dimethicone/Vinyl Dimethicone Crosspolymer, Aluminum Hydroxide, Stearic Acid, Camellia Sinensis Leaf Extract, Lavandula Hybrida Oil, Ascorbyl Tetraisopalmitate, Tocopheryl Acetate, Tocopherol, Dimethicone/PEG-10/15 Crosspolymer, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Caprylic/Capric Triglyceride, Sodium DNA, Sodium Hyaluronate, Sodium PCA, Dipotassium Glycyrrhizate, Silica, Carbomer, Sodium Chloride, Sodium Citrate, Linalool, Tetrasodium EDTA, Phenoxyethanol, Methylparaben, Propylparaben.

warnings

For external use only, not to be swallowed.

Avoid contact with eyes. If contact occurs, flush thoroughly with water.

If irritation develops, discontinue use.

Do not use on infants under 6 months old.

PRINCIPAL DISPLAY PANEL - 50 ml Carton

super
sensitive
faceblock

spf 30

NPN# 80005547
AUS L 138151

1.7 FL OZ / 50 ml e

dermalogica®

INGREDIENTS AND APPEARANCE

FACEBLOCK   SPF30 SUPER SENSITIVE
titanium dioxide and zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21839-111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Titanium Dioxide (UNII: 15FIX9V2JP) (Titanium Dioxide - UNII:15FIX9V2JP)	Titanium Dioxide	3.35 mL  in 50 mL
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z)	Zinc Oxide	4.6 mL  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Cyclomethicone 5 (UNII: 0THT5PCI0R)
Dimethicone (UNII: 92RU3N3Y1O)
Butylene Glycol (UNII: 3XUS85K0RA)
Dicaprylyl Ether (UNII: 77JZM5516Z)
Aluminum Hydroxide (UNII: 5QB0T2IUN0)
Stearic Acid (UNII: 4ELV7Z65AP)
Green Tea Leaf (UNII: W2ZU1RY8B0)
Lavandin Oil (UNII: 9RES347CKG)
Alpha-Tocopherol (UNII: H4N855PNZ1)
Medium-Chain Triglycerides (UNII: C9H2L21V7U)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Silicon Dioxide (UNII: ETJ7Z6XBU4)
Sodium Chloride (UNII: 451W47IQ8X)
Sodium Citrate (UNII: 1Q73Q2JULR)
Linalool, Dl- (UNII: D81QY6I88E)
Edetate Sodium (UNII: MP1J8420LU)
Phenoxyethanol (UNII: HIE492ZZ3T)
Methylparaben (UNII: A2I8C7HI9T)
Propylparaben (UNII: Z8IX2SC1OH)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21839-111-50	1 in 1 BOX
1		50 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	11/09/2005

Labeler - Gordon Laboratories, Inc (008328619)