Label: SUNSCREEN- avobenzone, homosalate, octisalat, octocrylene lotion
- NDC Code(s): 11822-0922-2
- Packager: Rite Aid
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 25, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Uses
- Warnings
- Do not use
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Directions
- apply liberally 15 minutes before sun exposure
- apply to all skin exposed to the sun
- reapply: after 80 minute of swimming or sweating
- immediately after towel drying
- at least every 2 hours
- Sun Protection Measures. Spending time in the sun increases your rist 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
- childre under 6 months of age: ask a doctor
- Other information
- Inactive ingredients
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ADVERSE REACTIONS
May stain or damage some fabrics or surfaces
DISTRIBUTED BY: RITE AID
30 HUNTER LAME
CAMP HIL, PA 17011
SATISFACTION GUARANTEE:
If you're not satisfied, we'll happily
refund your money.
*This product is not manufactured or distributed by Johnson & Johnson Consumer, Inc., distributor of Neutrogena Ultra Sheer Dry-Touch Sunscreen Broad Spectrum SPF 100
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INGREDIENTS AND APPEARANCE
SUNSCREEN
avobenzone, homosalate, octisalat, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0922 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 HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 150 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM) STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) YELLOW WAX (UNII: 2ZA36H0S2V) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) CHLORPHENESIN (UNII: I670DAL4SZ) BENZYL ALCOHOL (UNII: LKG8494WBH) TROLAMINE (UNII: 9O3K93S3TK) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0922-2 88 mL in 1 TUBE; Type 0: Not a Combination Product 11/30/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 11/30/2021 Labeler - Rite Aid (014578892) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(11822-0922) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091520 manufacture(11822-0922)
