Label: HOPE IN A JAR BROAD SPECTRUM SPF 25 SUNSCREEN AND MOISTURIZER FOR ALL SKIN TYPES- avobenzone, homosalate, octisalate, octocrylene, oxybenzone cream
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Contains inactivated NDC Code(s)
NDC Code(s): 50184-1032-1, 50184-1032-2 - Packager: Philosophy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated April 17, 2013
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Keep out of reach of children.
- Uses
- Warnings
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Directions
- apply liberally 15 minutes before sun exposure
- reapply at least ever 2 hours
- use a water resistant sunscreen if swimming or sweating
- Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regulalry use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measures, including:
- limit time in the sun, especially from 10 a.m.-2p.m.
- wear long-sleeve shirts, pants, hats and sunglasses
- children under 6 months: ask a doctor--this product should NOT be sued on children of any age
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Inactive Ingredients
water, butyloctyl salicylate, dibutyl adipate, glycerin, diethylhexyl syringlidenemalonate, cetearyl alcohol, cetearyl glucoside, potassium cetyl phosphate, behenoxy dimethicone, behenyl alcohol, hydroxyethnyl acrylate/sodium acryloyldimethyl taurate copolymer, cyclopentasiloxane, cyclohexasiloxane, beta-glucan, tocopheryl acetate, retinyl palmitate, lavandula angustifolia (lavendar oil), lauryl lactate, panthenol, arginine, lactic acid, capric/caprylic triglyceride, hydrogenated palm glycerides, xanthan gum, benzyl alcohl, disodium edta, polysorbate 60, sorbitan isostearate, chlorphenesin, phenoxyethanol, caprylyl glycol, potassium sorbate, hexylene glycol.
- Other Information
- Questions or Comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HOPE IN A JAR BROAD SPECTRUM SPF 25 SUNSCREEN AND MOISTURIZER FOR ALL SKIN TYPES
avobenzone, homosalate, octisalate, octocrylene, oxybenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50184-1032 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Avobenzone (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) Avobenzone 2.088 g in 60 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 2.838 g in 60 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 3.041 g in 60 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 1.733 g in 60 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 3.96 g in 60 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) DIBUTYL ADIPATE (UNII: F4K100DXP3) GLYCERIN (UNII: PDC6A3C0OX) DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) CYCLOMETHICONE 6 (UNII: XHK3U310BA) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) LAVENDER OIL (UNII: ZBP1YXW0H8) LAURYL LACTATE (UNII: G5SU0BFK7O) PANTHENOL (UNII: WV9CM0O67Z) ARGININE (UNII: 94ZLA3W45F) LACTIC ACID (UNII: 33X04XA5AT) TRICAPRIN (UNII: O1PB8EU98M) HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q) XANTHAN GUM (UNII: TTV12P4NEE) BENZYL ALCOHOL (UNII: LKG8494WBH) EDETATE DISODIUM (UNII: 7FLD91C86K) POLYSORBATE 60 (UNII: CAL22UVI4M) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) CHLORPHENESIN (UNII: I670DAL4SZ) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) HEXYLENE GLYCOL (UNII: KEH0A3F75J) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50184-1032-2 1 in 1 BOX 1 NDC:50184-1032-1 60 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 02/01/2013 Labeler - Philosophy (948102256) Establishment Name Address ID/FEI Business Operations Bio Tech Research Labs 948102256 manufacture(50184-1032)