Label: 70 DRY TOUCH SPF 70- avobenzone 3% homosalate 15% octisalate 5% octocrylene 10% oxybenzone 3% stick
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Contains inactivated NDC Code(s)
NDC Code(s): 0363-1125-01 - Packager: Walgreens
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 July 19, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions
Remove cap and twist up tube.
See important warnings under "When using this
product" • apply liberally 15 minutes before sun
exposure • 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,egularly use a sunscreen with a broad spectrum
SPF 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 - INACTIVE INGREDIENT
- Questions? 1-800-925-4733
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
70 DRY TOUCH SPF 70
avobenzone 3% homosalate 15% octisalate 5% octocrylene 10% oxybenzone 3% stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-1125 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Avobenzone (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) Avobenzone 3 g in 100 g Homosalate (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) Homosalate 15 g in 100 g Octisalate (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) Octisalate 5 g in 100 g Octocrylene (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) Octocrylene 10 g in 100 g Oxybenzone (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) Oxybenzone 3 g in 100 g Inactive Ingredients Ingredient Name Strength YELLOW WAX (UNII: 2ZA36H0S2V) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) Caprylyl Glycol (UNII: 00YIU5438U) NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C) Neopentyl Glycol Diisostearate (UNII: 4M6OQ34JWW) Octyldodecyl Neopentanoate (UNII: X8725R883T) CERESIN (UNII: Q1LS2UJO3A) Paraffin (UNII: I9O0E3H2ZE) Petrolatum (UNII: 4T6H12BN9U) POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-1125-01 43 g in 1 PACKAGE; Type 0: Not a Combination Product 12/07/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 12/07/2015 Labeler - Walgreens (008965063) Registrant - Product Quiest Mfg (927768135) Establishment Name Address ID/FEI Business Operations Product Quiest Mfg 927768135 manufacture(0363-1125) , label(0363-1125)
