SKIN CRAVE BROAD SPECTRUM SPF30- spf30 broad spectrum sunscreen lotion lotion

Skin Crave Broad Spectrum spf30 by

Drug Labeling and Warnings

Skin Crave Broad Spectrum spf30 by is a Otc medication manufactured, distributed, or labeled by Tropical Enterprises International Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Directions: Apply liberally and evenly 15 minutes before sun exposure.

Reapply every 2 hours as needed, after 40 minutes of swimming or sweating, or immediately after towel drying.

INACTIVE INGREDIENT

Inactive Ingredients:

Water, Polyester-7, Neopentyl Glycol Diheptanoate, Triethanolamine, Hypromellose, Acrylic Polymer, Propylene Glycol, Diazolidinyl Urea, Methylparaben, Propylparaben, Disodium EDTA

INDICATIONS & USAGE

Uses: Helps prevent sunburn. If used as direted with other sun protection measures, decreases the risk of skin cancer and eraly aging caused by the sun.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If product is swallowed, seek immediate medical attention or contact a Poison Control Center right away.

PURPOSE

Purpose: Sunscreen

WARNINGS

WARNINGS:

For external use only.

When using this product avoid contact with eyes. If contact with eyes occurs, flush with water to remove.

Stop use and ask a doctor if irritation or rash develops and persists.

Keep out of reach of children. If products is swalled, seek immediate medical attention or contact a Poison Control Center right away.

ACTIVE INGREDIENT

Active Ingredients:

Octocrylene 10%

Homosalate 10%

Oxybenzone 6%

Octisalate 5%

Avobenzone 3%

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SKIN CRAVE BROAD SPECTRUM SPF30 
spf30 broad spectrum sunscreen lotion lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58418-224
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	10 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	10 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	6 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POLYESTER-7 (UNII: 0841698D2F)
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
HYPROMELLOSE 2208 (100 MPA.S) (UNII: B1QE5P712K)
CUPRIC TRIETHANOLAMINE (UNII: 6NU949U74E)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58418-224-10	10 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2012
2	NDC: 58418-224-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2012
3	NDC: 58418-224-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2012
4	NDC: 58418-224-04	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2012
5	NDC: 58418-224-12	360 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/01/2012
6	NDC: 58418-224-64	1920 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/01/2012
7	NDC: 58418-224-28	3840 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/01/2012
8	NDC: 58418-224-08	240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/01/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	08/01/2012

Labeler - Tropical Enterprises International Inc (091986179)

Registrant - Tropical Enterprises International Inc (091986179)