Label: CARING MILL KIDS SUNSCREEN SPF 50- avobenzone, homosalate, octisalate, liquid
- NDC Code(s): 81522-954-01
- Packager: FSA Store Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 12, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Uses
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Warnings
For external use only
Flammable:Do not use near heat, flame, or while smoking
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Directions
- Shake well before each use
- Spray liberally and spread evenly by hand 15 minutes before sun exposure
- Hold container 4 to 6 inches from the skin to apply
- Do not spray directly into face. Spray on hands then apply to face.
- Do not apply in windy conditions
- Use in a well-ventilated area
- Reapply
- After 80 minutes of swimming or sweating
- Immediateky 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 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-sleeve shirts, pants, hats, and sunglasses
- Children under 6 months: Ask a doctor
- Other information
- Inactive ingredients
- Package Labeling:
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INGREDIENTS AND APPEARANCE
CARING MILL KIDS SUNSCREEN SPF 50
avobenzone, homosalate, octisalate, liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81522-954 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 100 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI) ASCORBYL PALMITATE (UNII: QN83US2B0N) ALCOHOL (UNII: 3K9958V90M) NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81522-954-01 162 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/20/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/20/2024 Labeler - FSA Store Inc. (049283340)