SHISEIDO SUN PROTECTION FOUNDATION SP10- titanium dioxide cream SHISEIDO SUN PROTECTION FOUNDATION SP20- titanium dioxide cream SHISEIDO SUN PROTECTION FOUNDATION SP30- titanium dioxide cream SHISEIDO SUN PROTECTION FOUNDATION SP40- titanium dioxide cream SHISEIDO SUN PROTECTION FOUNDATION SP50- titanium dioxide cream SHISEIDO SUN PROTECTION FOUNDATION SP60- titanium dioxide cream SHISEIDO SUN PROTECTION FOUNDATION SP70- titanium dioxide cream

SHISEIDO SUN PROTECTION FOUNDATION by

Drug Labeling and Warnings

SHISEIDO SUN PROTECTION FOUNDATION by is a Otc medication manufactured, distributed, or labeled by SHISEIDO AMERICA INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

TITANIUM DIOXIDE 4.1%

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

For sunscreen use:

• apply liberally 15 minutes before sun exposure
• reapply:
  • after 80 minutes of swimming or sweating
  • immediately after towel drying
  • at least every 2 hours
• Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:
  • limit time in the sun, especially from 10 a.m. – 2 p.m.
  • wear long-sleeve shirts, pants, hats, and sunglasses
• children under 6 months: Ask a doctor

Inactive Ingredients

CYCLOMETHICONE, WATER, TRIMETHYLSILOXYSILICATE, TALC, DIPROPYLENE GLYCOL, PEG/PPG-19/19 DIMETHICONE, PHYTOSTERYL/OCTYLDODECYL LAUROYL GLUTAMATE, ZINC MYRISTATE, TOCOPHERYL ACETATE, THIOTAURINE, STEARYL GLYCYRRHETINATE, ETHYLHEXYL METHOXYCINNAMATE, ISOSTEARIC ACID, ALUMINUM DISTEARATE, ALUMINUM HYDROXIDE, CALCIUM STEARATE, TRIETHOXYCAPRYLYLSILANE, GLYCERIN, POLYSILICONE-2, SODIUM CITRATE, TOCOPHEROL, PALMITIC ACID, DISTEARYLDIMONIUM CHLORIDE, TRISODIUM EDTA, ISOPROPYL ALCOHOL, BHT, METHYLPARABEN, FRAGRANCE, TITANIUM DIOXIDE, IRON OXIDES

Other information

• protect this product in this container from excessive heat and direct sun.

Questions or comments?

Call toll free 1-800-906-7503

SPL UNCLASSIFIED SECTION

SHISEIDO AMERICA INC. NEW YORK, N.Y. 10022
SHISEIDO DIST. NEW YORK PARIS MILANO

PRINCIPAL DISPLAY PANEL - 30mL Bottle Carton - SP10

SHISEIDO

42

Sun Protection
Liquid Foundation

BROAD SPECTRUM
SPF 42

WATER RESISTANT
(80 MINUTES)

SUNSCREEN

30mL 1 FL. OZ.

PRINCIPAL DISPLAY PANEL - 30mL Bottle Carton - SP20

SHISEIDO

42

Sun Protection
Liquid Foundation

BROAD SPECTRUM
SPF 42

WATER RESISTANT
(80 MINUTES)

SUNSCREEN

30mL 1 FL. OZ.

PRINCIPAL DISPLAY PANEL - 30mL Bottle Carton - SP30

SHISEIDO

42

Sun Protection
Liquid Foundation

BROAD SPECTRUM
SPF 42

WATER RESISTANT
(80 MINUTES)

SUNSCREEN

30mL 1 FL. OZ.

PRINCIPAL DISPLAY PANEL - 30mL Bottle Carton - SP40

SHISEIDO

42

Sun Protection
Liquid Foundation

BROAD SPECTRUM
SPF 42

WATER RESISTANT
(80 MINUTES)

SUNSCREEN

30mL 1 FL. OZ.

PRINCIPAL DISPLAY PANEL - 30mL Bottle Carton - SP50

SHISEIDO

42

Sun Protection
Liquid Foundation

BROAD SPECTRUM
SPF 42

WATER RESISTANT
(80 MINUTES)

SUNSCREEN

30mL 1 FL. OZ.

PRINCIPAL DISPLAY PANEL - 30mL Bottle Carton - SP60

SHISEIDO

42

Sun Protection
Liquid Foundation

BROAD SPECTRUM
SPF 42

WATER RESISTANT
(80 MINUTES)

SUNSCREEN

30mL 1 FL. OZ.

PRINCIPAL DISPLAY PANEL - 30mL Bottle Carton - SP70

SHISEIDO

42

Sun Protection
Liquid Foundation

BROAD SPECTRUM
SPF 42

WATER RESISTANT
(80 MINUTES)

SUNSCREEN

30mL 1 FL. OZ.

INGREDIENTS AND APPEARANCE

SHISEIDO SUN PROTECTION FOUNDATION  SP10
titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52686-264
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1488 mg  in 36.3 g

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE (UNII: NMQ347994Z)
WATER (UNII: 059QF0KO0R)
TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
TALC (UNII: 7SEV7J4R1U)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
PEG/PPG-19/19 DIMETHICONE (UNII: EHH90CO7TL)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
OCTINOXATE (UNII: 4Y5P7MUD51)
ISOSTEARIC ACID (UNII: X33R8U0062)
ALUMINUM DISTEARATE (UNII: 7P1HP1B9UI)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
CALCIUM STEARATE (UNII: 776XM7047L)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
METHYLPARABEN (UNII: A2I8C7HI9T)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
ZINC MYRISTATE (UNII: K09A9E2GGO)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
PALMITIC ACID (UNII: 2V16EO95H1)
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
EDETATE TRISODIUM (UNII: 420IP921MB)
STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P)
THIOTAURINE (UNII: NQZ2D7AO62)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52686-264-10	1 in 1 CARTON	01/01/2004
1		36.3 g 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	01/01/2004

SHISEIDO SUN PROTECTION FOUNDATION  SP20
titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52686-265
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1488 mg  in 36.3 g

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE (UNII: NMQ347994Z)
WATER (UNII: 059QF0KO0R)
TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
TALC (UNII: 7SEV7J4R1U)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
PEG/PPG-19/19 DIMETHICONE (UNII: EHH90CO7TL)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
OCTINOXATE (UNII: 4Y5P7MUD51)
ISOSTEARIC ACID (UNII: X33R8U0062)
ALUMINUM DISTEARATE (UNII: 7P1HP1B9UI)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
CALCIUM STEARATE (UNII: 776XM7047L)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
METHYLPARABEN (UNII: A2I8C7HI9T)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
ZINC MYRISTATE (UNII: K09A9E2GGO)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
PALMITIC ACID (UNII: 2V16EO95H1)
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
EDETATE TRISODIUM (UNII: 420IP921MB)
STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P)
THIOTAURINE (UNII: NQZ2D7AO62)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52686-265-10	1 in 1 CARTON	01/01/2004
1		36.3 g 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	01/01/2004

SHISEIDO SUN PROTECTION FOUNDATION  SP30
titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52686-266
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1488 mg  in 36.3 g

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE (UNII: NMQ347994Z)
WATER (UNII: 059QF0KO0R)
TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
TALC (UNII: 7SEV7J4R1U)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
PEG/PPG-19/19 DIMETHICONE (UNII: EHH90CO7TL)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
OCTINOXATE (UNII: 4Y5P7MUD51)
ISOSTEARIC ACID (UNII: X33R8U0062)
ALUMINUM DISTEARATE (UNII: 7P1HP1B9UI)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
CALCIUM STEARATE (UNII: 776XM7047L)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
METHYLPARABEN (UNII: A2I8C7HI9T)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
ZINC MYRISTATE (UNII: K09A9E2GGO)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
PALMITIC ACID (UNII: 2V16EO95H1)
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
EDETATE TRISODIUM (UNII: 420IP921MB)
STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P)
THIOTAURINE (UNII: NQZ2D7AO62)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52686-266-10	1 in 1 CARTON	01/01/2004
1		36.3 g 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	01/01/2004

SHISEIDO SUN PROTECTION FOUNDATION  SP40
titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52686-267
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1488 mg  in 36.3 g

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE (UNII: NMQ347994Z)
WATER (UNII: 059QF0KO0R)
TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
TALC (UNII: 7SEV7J4R1U)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
PEG/PPG-19/19 DIMETHICONE (UNII: EHH90CO7TL)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
OCTINOXATE (UNII: 4Y5P7MUD51)
ISOSTEARIC ACID (UNII: X33R8U0062)
ALUMINUM DISTEARATE (UNII: 7P1HP1B9UI)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
CALCIUM STEARATE (UNII: 776XM7047L)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
METHYLPARABEN (UNII: A2I8C7HI9T)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
ZINC MYRISTATE (UNII: K09A9E2GGO)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
PALMITIC ACID (UNII: 2V16EO95H1)
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
EDETATE TRISODIUM (UNII: 420IP921MB)
STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P)
THIOTAURINE (UNII: NQZ2D7AO62)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52686-267-10	1 in 1 CARTON	01/01/2004
1		36.3 g 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	01/01/2004

SHISEIDO SUN PROTECTION FOUNDATION  SP50
titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52686-268
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1488 mg  in 36.3 g

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE (UNII: NMQ347994Z)
WATER (UNII: 059QF0KO0R)
TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
TALC (UNII: 7SEV7J4R1U)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
PEG/PPG-19/19 DIMETHICONE (UNII: EHH90CO7TL)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
OCTINOXATE (UNII: 4Y5P7MUD51)
ISOSTEARIC ACID (UNII: X33R8U0062)
ALUMINUM DISTEARATE (UNII: 7P1HP1B9UI)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
CALCIUM STEARATE (UNII: 776XM7047L)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
METHYLPARABEN (UNII: A2I8C7HI9T)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
ZINC MYRISTATE (UNII: K09A9E2GGO)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
PALMITIC ACID (UNII: 2V16EO95H1)
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
EDETATE TRISODIUM (UNII: 420IP921MB)
STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P)
THIOTAURINE (UNII: NQZ2D7AO62)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52686-268-10	1 in 1 CARTON	01/01/2004
1		36.3 g 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	01/01/2004

SHISEIDO SUN PROTECTION FOUNDATION  SP60
titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52686-269
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1488 mg  in 36.3 g

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE (UNII: NMQ347994Z)
WATER (UNII: 059QF0KO0R)
TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
TALC (UNII: 7SEV7J4R1U)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
PEG/PPG-19/19 DIMETHICONE (UNII: EHH90CO7TL)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
OCTINOXATE (UNII: 4Y5P7MUD51)
ISOSTEARIC ACID (UNII: X33R8U0062)
ALUMINUM DISTEARATE (UNII: 7P1HP1B9UI)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
CALCIUM STEARATE (UNII: 776XM7047L)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
METHYLPARABEN (UNII: A2I8C7HI9T)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
ZINC MYRISTATE (UNII: K09A9E2GGO)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
PALMITIC ACID (UNII: 2V16EO95H1)
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
EDETATE TRISODIUM (UNII: 420IP921MB)
STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P)
THIOTAURINE (UNII: NQZ2D7AO62)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52686-269-10	1 in 1 CARTON	01/01/2004
1		36.3 g 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	01/01/2004

SHISEIDO SUN PROTECTION FOUNDATION  SP70
titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52686-270
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1488 mg  in 36.3 g

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE (UNII: NMQ347994Z)
WATER (UNII: 059QF0KO0R)
TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
TALC (UNII: 7SEV7J4R1U)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
PEG/PPG-19/19 DIMETHICONE (UNII: EHH90CO7TL)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
OCTINOXATE (UNII: 4Y5P7MUD51)
ISOSTEARIC ACID (UNII: X33R8U0062)
ALUMINUM DISTEARATE (UNII: 7P1HP1B9UI)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
CALCIUM STEARATE (UNII: 776XM7047L)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
METHYLPARABEN (UNII: A2I8C7HI9T)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
ZINC MYRISTATE (UNII: K09A9E2GGO)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
PALMITIC ACID (UNII: 2V16EO95H1)
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
EDETATE TRISODIUM (UNII: 420IP921MB)
STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P)
THIOTAURINE (UNII: NQZ2D7AO62)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52686-270-10	1 in 1 CARTON	01/01/2004
1		36.3 g 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	01/01/2004

Labeler - SHISEIDO AMERICA INC. (782677132)

Establishment
Name	Address	ID/FEI	Business Operations
SHISEIDO AMERICA INC.		782677132	manufacture(52686-264, 52686-265, 52686-266, 52686-267, 52686-268, 52686-269, 52686-270) , analysis(52686-264, 52686-265, 52686-266, 52686-267, 52686-268, 52686-269, 52686-270)