DOLCE AND GABBANA THE LIFT FOUNDATION WARM ROSE 130- octinoxate, titanium dioxide liquid

Dolce and Gabbana The Lift Foundation Warm Rose 130 by

Drug Labeling and Warnings

Dolce and Gabbana The Lift Foundation Warm Rose 130 by is a Otc medication manufactured, distributed, or labeled by Proter & Gamble Manufacturing Company, Nihon Kolmar Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

OCTINOXATE  2.99%
TITANIUM DIOXIDE  2.52%

Purpose

Sunscreen

Uses

• helps prevent sunburn
• if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun
  

Warnings

For external use only

Do not use

on damaged or broken skin

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

if rash occurs

Keep out of reach of children.

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

• apply liberally 15 minutes before sun exposure
• reapply at least every 2 hours
• use water resistant sunscreen if swimming or sweating
• Sun Protection Measures. increases your risk of skin cancer and early skin aging.  To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
• • limit time in sun, especially from 10 a.m. – 2 p.m.
  • wear long-sleeved shirts, pants, hats, and sunglasses
• children under 6 months: ask a doctor
  

Other information

• protect this product from excessive heat and direct sun

Inactive ingredients

water, cyclopentasiloxane, diphenylsiloxy phenyl trimethicone, butylene glycol, niacinamide, PEG-9 polydimethylsiloxyethyl dimethicone, triethylhexanoin, talc, glycerin, disteardimonium hectorite, cetyl PEG/PPG-10/1 dimethicone, panthenol, sodium chloride, trimethylsiloxysilicate, vinyl dimethicone/methicone silsesquioxane crosspolymer, tocopherol, phytosteryl/octyldodecyl lauroyl glutamate, tribehenin, phytosteryl/behenyl/octyldodecyl lauroyl glutamate, aluminum hydroxide, hydrated silica, dimethicone, hydrogen dimethicone, dimethicone/vinyl dimethicone crosspolymer, olea europaea (olive) fruit oil, hydrolyzed silk, simmondsia chinensis (jojoba) seed extract, phenoxyethanol, methylparaben, sodium benzoate, propylparaben, titanium dioxide, iron oxides

Questions or comments?

1-866-607-0858

PRINCIPAL DISPLAY PANEL

DOLCE AND GABBANA 

THE LIFT FOUNDATION 

PERFECT
REVEAL LIFT
FOUNDATION
WITH SUNSCREEN

BROAD SPECTRUM SPF 25 

30ml / 1 fl oz 

P&G PRESTIGE BEAUTE 
LONDON ECIA 4DD, UK  

MADE IN JAPAN 

WARM ROSE 130

Product Labels

INGREDIENTS AND APPEARANCE

DOLCE AND GABBANA THE LIFT FOUNDATION WARM ROSE 130 
octinoxate, titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37000-914
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	29.9 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	25.2 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIPHENYLSILOXY PHENYL TRIMETHICONE (UNII: I445L28B12)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
NIACINAMIDE (UNII: 25X51I8RD4)
PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: TYP81E471F)
TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
TALC (UNII: 7SEV7J4R1U)
GLYCERIN (UNII: PDC6A3C0OX)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
PANTHENOL (UNII: WV9CM0O67Z)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
TOCOPHEROL (UNII: R0ZB2556P8)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
DIMETHICONE (UNII: 92RU3N3Y1O)
OLIVE OIL (UNII: 6UYK2W1W1E)
SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
METHYLPARABEN (UNII: A2I8C7HI9T)
SODIUM BENZOATE (UNII: OJ245FE5EU)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
FERRIC OXIDE RED (UNII: 1K09F3G675)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37000-914-30	1 in 1 CARTON	04/05/2014
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	04/05/2014

Labeler - Proter & Gamble Manufacturing Company (004238200)

Establishment
Name	Address	ID/FEI	Business Operations
Nihon Kolmar Co., Ltd.		717820687	manufacture(37000-914)