Label: PRO-TECT SPORTS SUNSCREEN SPF 20- meradimate, octinoxate, octisalate, oxybenzone lotion
- NDC Code(s): 68605-8640-2, 68605-8640-4, 68605-8640-8
- Packager: ABBE Laboratories, Inc.
- This is a repackaged label.
- Source NDC Code(s): 37945-862
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 13, 2026
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- 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
•children under 6 months: 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 10a.m.–2 p.m.
•wear long-sleeved shirts, pants, hats, and sun-glasses - Other Information
- Inactive Ingredients
- Questions or Comments
- Package Label
-
INGREDIENTS AND APPEARANCE
PRO-TECT SPORTS SUNSCREEN SPF 20
meradimate, octinoxate, octisalate, oxybenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68605-8640(NDC:37945-862) Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 g MERADIMATE (UNII: J9QGD60OUZ) (MERADIMATE - UNII:J9QGD60OUZ) MERADIMATE 50 mg in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 30 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) BENZYL ALCOHOL (UNII: LKG8494WBH) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) CETYL ALCOHOL (UNII: 936JST6JCN) CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36) CETYL DIMETHICONE 45 (UNII: IK315POC44) DIETHANOLAMINE CETYL PHOSPHATE (UNII: 4UG0316V9S) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) STEARIC ACID (UNII: 4ELV7Z65AP) TALC (UNII: 7SEV7J4R1U) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68605-8640-4 113.4 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/01/2022 2 NDC:68605-8640-8 226.8 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/01/2022 3 NDC:68605-8640-2 907.2 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 05/01/2022 Labeler - ABBE Laboratories, Inc. (781745286) Establishment Name Address ID/FEI Business Operations ABBE Laboratories, Inc. 781745286 repack(68605-8640)
