Label: CROC BLOC BROAD SPECTRUM SPF 30 FPS ECRAN SOLAIRE- homosalate, octisalate, octocrylene, oxybenzone, and avobenzone lotion
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NDC Code(s):
58331-030-01,
58331-030-02,
58331-030-03,
58331-030-04, view more58331-030-05
- Packager: Degil Safety Products (1989) Inc.
- Category: HUMAN OTC DRUG LABEL
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 November 21, 2022
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Warnings
- Directions
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Other Ingredients
Aqua, Sorbitan Isostearate, Sorbitol, Triethanolamine, Polyglyceryl-3 Distearate, Stearic Acid, Octadecene/MA Copolymer, Barium Sulfate, Benzyl Alcohol, VP/Eicosene Copolymer, Dimethicone, Carbomer, Methyl-paraben, Aloe Barbadensis Leaf Extract, Simmondsia Chinesis (Jojoba) Seed Oil, Tocopherol, Propylparaben, Disodium EDTA
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PRINCIPAL DISPLAY PANEL - 120 mL Bottle Label
Sunscreen
SPF 30 FPS
Écran Solaire
BROAD SPECTRUM • LARGE SPECTRE
UVA/UVB PROTECTIONCONTRE LES RAYONS UVA ET UVB
Dermatologist Tested • Moisturizing Aloe & Vitamin E
Unscented Lotion • Water Sweat Resistant (40 Minutes)
Testé par les dermatologues • Hydratante avec Vitamine E et AloésLotion Non Parfumée • Résiste à l'eau
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INGREDIENTS AND APPEARANCE
CROC BLOC BROAD SPECTRUM SPF 30 FPS ECRAN SOLAIRE
homosalate, octisalate, octocrylene, oxybenzone, and avobenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58331-030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 10.5 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 2 g in 100 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 2 g in 100 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) SORBITOL (UNII: 506T60A25R) TROLAMINE (UNII: 9O3K93S3TK) POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV) STEARIC ACID (UNII: 4ELV7Z65AP) BARIUM SULFATE (UNII: 25BB7EKE2E) BENZYL ALCOHOL (UNII: LKG8494WBH) DIMETHICONE (UNII: 92RU3N3Y1O) CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E) METHYLPARABEN (UNII: A2I8C7HI9T) ALOE VERA LEAF (UNII: ZY81Z83H0X) JOJOBA OIL (UNII: 724GKU717M) TOCOPHEROL (UNII: R0ZB2556P8) PROPYLPARABEN (UNII: Z8IX2SC1OH) EDETATE DISODIUM (UNII: 7FLD91C86K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58331-030-01 120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/21/2022 2 NDC:58331-030-02 10 mL in 1 PACKET; Type 0: Not a Combination Product 11/21/2022 3 NDC:58331-030-03 30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/21/2022 4 NDC:58331-030-04 180 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/21/2022 5 NDC:58331-030-05 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/21/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 05/15/2013 Labeler - Degil Safety Products (1989) Inc. (247083686) Registrant - CSR Cosmetic Solutions (243501959)