In An Instant Daily Tinted Moisturizer, SPF 15

In An Instant by

Drug Labeling and Warnings

In An Instant by is a Otc medication manufactured, distributed, or labeled by Guthy-Renker LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

IN AN INSTANT  DAILY TINTED MOISTURIZER SPF 15- octinoxate, octisalate, and avobenzone cream 
THE PROACTIV COMPANY LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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In An Instant Daily Tinted Moisturizer, SPF 15

Drug Facts

Uses

Helps prevent sunburn. Higher SPF gives more sunburn protection.

Directions

Apply evenly onto face in the morning, before sun exposure and as needed. Tint will appear as you apply the lotion, acting as an indicator of complete and even coverage. Children under 6 months of age: ask a doctor.

WARNINGS

For external use only. Avoid contact with eyes. If contact occurs, flush gently and thoroughly with water.

Discontinue use if rash or irritation occurs.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Sun alert

Limiting sun exposure, wearing protective clothing and using sunscreens may reduce the risks of skin aging, skin cancer and other harmful effects of the sun.

ACTIVE INGREDIENTS

OCTINOXATE 7.5%, OCTISALATE 5%, AVOBENZONE 2%

INACTIVE INGREDIENTS

WATER (AQUA), DIMETHICONE, CAPRYLlC/CAPRIC/MYRISTIC/STEARIC TRIGLYCERIDE, CYCLOPENTASILOXANE, BUTYLENE GLYCOL, STEARETH-2, POLYSILICONE-11, CETYL RICINOLEATE, DI-C12-15 ALKYL FUMARATE, PENTYLENE GLYCOL, STEARETH-21, POLYETHYLENE, COFFEA ARABICA (COFFEE) SEED EXTRACT, ROSMARINUS OFFICINALIS (ROSEMARY) EXTRACT, ISOPROPYL MYRISTATE, VITIS VINIFERA (GRAPE) SEED EXTRACT, HORDEUM VULGARE EXTRACT, TRITICUM VULGARE (WHEAT) GERM EXTRACT, LAMINARIA OCHROLEUCA EXTRACT, ORYZANOL,CAMELLIA SINENSIS LEAF EXTRACT, ASPALATHUS LlNEARIS LEAF EXTRACT, POLYGONUM CUSPIDATUM ROOT EXTRACT, BETULA ALBA BARK EXTRACT, SACCHAROMYCES LYSATE EXTRACT, ASCORBYL TOCOPHERYL MALEATE, STEARYL ALCOHOL, TROMETHAMINE, GLYCERIN, CARBOMER, PHOSPHOLIPIDS, BENZYL ALCOHOL, POLYMETHYL METHACRYLATE, DISODIUM EDTA, LlNOLEIC ACID, CHOLESTEROL, BEHENYL ALCOHOL, SQUALANE, SODIUM PCA, SODIUM DEHYDROACETATE, CAPRYLIC/CAPRIC TRIGLYCERIDE, PANTETHINE, SODIUM HYDROXIDE, UREA, VP/HEXADECENE COPOLYMER, TREHALOSE, SODIUM HYALURONATE, POLYQUATERNIUM-51, PALMITOYL HYDROXYPROPYLTRIMONIUM AMYLOPECTIN/GLYCERIN CROSSPOLYMER, CYCLODEXTRIN, MALTODEXTRIN, NORDIHYDROGUAIARETIC ACID, LINOLENIC ACID, LECITHIN, ETHYLBISIMINOMETHYLGUAIACOL MANGANESE CHLORIDE, BHT, ETHYLPARABEN, ISOPROPYLPARABEN, BUTYLPARABEN, ISOBUTYLPARABEN, METHYLPARABEN, PROPYLPARABEN, PHENOXYETHANOL, FRAGRANCE (PARFUM), TITANIUM DIOXIDE (CI 77891), IRON OXIDES (CI 77491, CI 77492, CI 77499)

PRINCIPAL DISPLAY PANEL - 15mL Tube Label

in an instant™
HEIDI KLUM

Instant Daily
Tinted Moisturizer
SPF 15

hydrates and protects
with a sheer tint

0.5 fl. oz. / 15mL e

IN AN INSTANT   DAILY TINTED MOISTURIZER SPF 15
octinoxate, octisalate, and avobenzone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11410-749
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	0.075 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	0.05 mg  in 1 mL
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX)	Avobenzone	0.02 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11410-749-17	50 mL in 1 TUBE; Type 0: Not a Combination Product	10/25/2007	12/31/2019
2	NDC: 11410-749-03	15 mL in 1 TUBE; Type 0: Not a Combination Product	10/25/2007	12/31/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	10/25/2007	12/31/2019

Labeler - THE PROACTIV COMPANY LLC (080216357)

Registrant - THE PROACTIV COMPANY LLC (080216357)

Revised: 9/2010

Document Id: 8d5c28ee-2b81-4600-b06a-65bb25bfe751

34390-5

Set id: 9996b995-354d-444c-8db7-7d6552d85e21

Version: 2

Effective Time: 20100913