Label: TARGET GOODFELLOW AND CO SPF 30 FACE SCENT NO. 05 KELP AND SEA MINERAL- avobenzone, homosalate, octisalate, octocrylene lotion
- NDC Code(s): 11673-232-04
- Packager: TARGET CORPORATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 14, 2024
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
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Directions
- apply liberally 15 minutes before sun exposure
reapply:
- after 80 minutes of swimming or sweating
- immediately after towel drying
- at least every 2 hours
- 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
- Other information
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Inactive ingredients
water, TRIDECYL SALICYLATE, sorbitol, stearic acid, Aluminum Starch Octenylsuccinate, SODIUM HYDROXIDE, POLYETHYLOXAZOLINE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, tocopherol, FRUCTOOLIGOSACCHARIDES, BETA VULGARIS (BEET) ROOT EXTRACT, disodium edta, polyglyceryl-3 distearate, LINOLEIC ACID, LINOLENIC ACID,CAPRYLYL GLYCOL, PHENOXYETHANOL, ETHYLHEXYLGLYCERIN, BENTONITE, Sorbitan isostearate, OILIC ACID, PALMITIC ACID BENZYL ALCOHOL, FRAGRANCE
- Label
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INGREDIENTS AND APPEARANCE
TARGET GOODFELLOW AND CO SPF 30 FACE SCENT NO. 05 KELP AND SEA MINERAL
avobenzone, homosalate, octisalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-232 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 70 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 150 mg in 1 mL Inactive Ingredients Ingredient Name Strength TRIDECYL SALICYLATE (UNII: AZQ08K38Z1) LINOLEIC ACID (UNII: 9KJL21T0QJ) OLEIC ACID (UNII: 2UMI9U37CP) POLYETHYLOXAZOLINE (5000 MW) (UNII: HNX7574GTX) SORBITOL (UNII: 506T60A25R) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) STEARIC ACID (UNII: 4ELV7Z65AP) PALMITIC ACID (UNII: 2V16EO95H1) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) WATER (UNII: 059QF0KO0R) EDETATE DISODIUM (UNII: 7FLD91C86K) PHENOXYETHANOL (UNII: HIE492ZZ3T) BENZYL ALCOHOL (UNII: LKG8494WBH) BENTONITE (UNII: A3N5ZCN45C) BETA VULGARIS ROOT FRUCTOOLIGOSACCHARIDES (UNII: N2UDM48ZD6) BEET (UNII: N487KM8COK) POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-232-04 118 mL in 1 TUBE; Type 0: Not a Combination Product 08/19/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 08/19/2020 Labeler - TARGET CORPORATION (006961700)
