SPF 30 SUNSCREEN TOTTLE W CARABINER- avobenzone, oxybenzone, homosalate, octinoxate, octisalate lotion

SPF 30 Sunscreen Tottle w Carabiner by

Drug Labeling and Warnings

SPF 30 Sunscreen Tottle w Carabiner by is a Otc medication manufactured, distributed, or labeled by INNOVATION SPECIALTIES, CORETEX PRODUCTS INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients

Avobenzone 1%

Oxybenzone 3%

Homosalate 5 %

Octinoxate 7.5 %

Octisalate 5 %

PURPOSE

Purpose

Sunscreen

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Directions

Apply liberally (or generously) and every 15 minutes before sun exposure. Children under 6 months of age ask a doctor. 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 value 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-sleeved shirts, pants, hats, and sunglasses. Reapply at least every 2 hours. Use a water resistant sunscreen if swimming or sweating. Reapply after 80 min. of swimming or sweating. Immediately after towel drying.

WARNINGS

Warnings:

For external use only. Do not use on damaged or broken skin. when using this product keep out of eyes. In case of contact rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts. Keep out of reach of children, if swallowed get medical help or contact a Poison Control Center.

DOSAGE & ADMINISTRATION

Dosage and Administration

Apply liberally (or generously)15 minutes before sun exposure, and reapply as needed.

INACTIVE INGREDIENT

Inactive Ingredients

Water, Dimethyl Capramide, Dimethicone, C12-15 Alkyl Benzoate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Symphytum Officinale Leaf Extract, Tocopherol, Nasturium Officinale Extract, Chamomile Recutita Extract, Calendula Officinalis Flower Extract, Triethanolamine,  Propylparaben,  Phenoxyethanol, Glyceryl Stearate, Methylparaben, Ethylparaben, Butylparaben, Peg-100 Stearate, Isobutylparaben, Tetrasodium Edta, Carbomer, Acrylates, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SPF 30 SUNSCREEN TOTTLE W CARABINER 
avobenzone, oxybenzone, homosalate, octinoxate, octisalate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76138-202
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	1 g  in 100 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	3 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	5 g  in 100 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7.5 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
DIMETHICONE (UNII: 92RU3N3Y1O)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
COMFREY LEAF (UNII: DG4F8T839X)
TOCOPHEROL (UNII: R0ZB2556P8)
NASTURTIUM OFFICINALE (UNII: YH89GMV676)
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
TROLAMINE (UNII: 9O3K93S3TK)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
METHYLPARABEN (UNII: A2I8C7HI9T)
ETHYLPARABEN (UNII: 14255EXE39)
BUTYLPARABEN (UNII: 3QPI1U3FV8)
PEG-100 STEARATE (UNII: YD01N1999R)
ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
EDETATE SODIUM (UNII: MP1J8420LU)
CARBOMER HOMOPOLYMER TYPE A (UNII: F68VH75CJC)
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76138-202-04	44 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	12/01/2008

Labeler - INNOVATION SPECIALTIES (030837314)

Establishment
Name	Address	ID/FEI	Business Operations
CORETEX PRODUCTS INC		061944620	manufacture(76138-202)