Label: KROGER INVISIBLE SUNSCREEN SPF 40- avobenzone, homosalate, octisalate, octocrylene gel
- NDC Code(s): 30142-239-09
- Packager: THE KROGER COMPANY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 March 17, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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.
-
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
-
Inactive ingredients
aloe barbadensis leaf extract, Bis-vinyldimethicone/peg-10 dimethicone crosspolymer, butyloctyl salicylate, butyrospermum parkii (shea) butter, cetyl peg/ppg-10/1 dimethicone, citrus aurantium dulcis (orange) oil, dimethicone, dimethicone crosspolymer, dimethicone/vinyl dimethicone crosspolymer, disteardimonium hectorite, hexyl laurate, hydrated silica, isododecane, isohexadecane, lecithine, mineral oil, neopentyl glycol diethylhexanoate, phenoxyethanol, polyester-8, polyglyceryl-4 isostearate, polymethyl methacrylate, polymethylsilsequioxane, tocopherol
- Label
-
INGREDIENTS AND APPEARANCE
KROGER INVISIBLE SUNSCREEN SPF 40
avobenzone, homosalate, octisalate, octocrylene gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-239 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 110 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 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 DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) ISOHEXADECANE (UNII: 918X1OUF1E) MINERAL OIL (UNII: T5L8T28FGP) ORANGE OIL (UNII: AKN3KSD11B) DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMER (UNII: RSA9I561OK) POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11) PHENOXYETHANOL (UNII: HIE492ZZ3T) SHEA BUTTER (UNII: K49155WL9Y) ISODODECANE (UNII: A8289P68Y2) POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P) POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ALOE VERA LEAF (UNII: ZY81Z83H0X) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) HEXYL LAURATE (UNII: 4CG9F9W01Q) NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30142-239-09 89 mL in 1 TUBE; Type 0: Not a Combination Product 09/27/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M020 09/27/2019 Labeler - THE KROGER COMPANY (006999528)
