Label: SUNSCREEN- avobenzone, homosalate, octisalate, oxybenzone spray
- NDC Code(s): 30142-687-14, 30142-687-38
- Packager: The Kroger Co
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 11, 2024
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Use
- Warnings
- Flammable:
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
-
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
- 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 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
- children under 6 months of age: Ask a doctor
- Other information
- Inactive ingredients
-
SPL UNCLASSIFIED SECTION
Kroger Sport Clear Spray SPF 50 provides quick and easy coverage with broad spectrum protection. Its clear, specially formulated spray goes on at any angle. Water resistant formula provides protection in and out of the water for up to 80 minutes.
May stain or damage some fabrics or surfaces
*This product is not manufactured or distributed by Bayer, distributor of Coppertone Sport High Performance Sunscreen Continuous Spray UVA/UVB Broad Spectrum SPF 50.
Distributed by The Kroger Co. Cincinnati, Ohio 45202
Quality guarantee 800-632-6900 www.kroger.com
787.000/787AA
- principal display panel
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INGREDIENTS AND APPEARANCE
SUNSCREEN
avobenzone, homosalate, octisalate, oxybenzone sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-687 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 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 150 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 60 mg in 1 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) ACRYLIC ACID/ISOPHORONE DIISOCYANATE/PEG-27 COPOLYMER (UNII: R0R8I3X29J) ALOE VERA LEAF (UNII: ZY81Z83H0X) COCONUT OIL (UNII: Q9L0O73W7L) MINERAL OIL (UNII: T5L8T28FGP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30142-687-14 156 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/07/2017 2 NDC:30142-687-38 283 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/07/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 08/07/2017 Labeler - The Kroger Co (006999528) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091520 manufacture(30142-687) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(30142-687)