Label: NO-AD BROAD SPECTRUM SPF 50- avobenzone, homosalate, octisalate, octocrylene aerosol
- NDC Code(s): 13630-0281-5
- Packager: Prime Packaging Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 15, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
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Directions
• Shake well. 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 and avoid inhalation.
• Children under 6 months of age: ask a doctor
• 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 a broad spectrum SPF value of 15 or higher and other sun protection measures including:
• Limit time in the sun, especially from 10 am - 2 pm
• Wear long-sleeved shirts, pants, hats and sunglasses
- Inactive Ingredients
- Other Information
- NO-AD SPF 50 Sunscreen Spray
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INGREDIENTS AND APPEARANCE
NO-AD BROAD SPECTRUM SPF 50
avobenzone, homosalate, octisalate, octocrylene aerosolProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:13630-0281 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 41.85 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 41.85 mg in 1 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 83.7 mg in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 25.11 mg in 1 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) VINYL ACETATE (UNII: L9MK238N77) ISOBORNYL ACRYLATE (UNII: IX0PRH184P) MONOBUTYL MALEATE (UNII: F2LD7FVO1L) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Product Characteristics Color yellow (Colorless to Yellow) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:13630-0281-5 255 g in 1 CAN; Type 0: Not a Combination Product 09/17/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 09/17/2021 Labeler - Prime Packaging Inc (805987059) Registrant - Prime Packaging Inc (805987059) Establishment Name Address ID/FEI Business Operations Prime Enterprises 101946028 analysis(13630-0281) , label(13630-0281) , manufacture(13630-0281) , pack(13630-0281) Establishment Name Address ID/FEI Business Operations Prime Packaging Inc 805987059 label(13630-0281) , pack(13630-0281)
