Label: SUNSCREEN SETTING SPRITZ, SPF 45- sunscreen setting spray liquid
- NDC Code(s): 70000-1543-1
- Packager: Cardinal Health, inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 14, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
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WARNINGS
Warnings
For external use only Do not use on damaged or broken skin.
When using this product: keep out of eyes, Rinse with water to remove.
Stop use and ask a doctor if rash occurs.
Keep out of reach of children.lf swallowed, get medical help or contacta Poison Control
Center right away
Flammable. Do not spray near heat sparks, sources of ignition, or flames - STOP USE
- DO NOT USE
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
Directions
Apply liberally 15 minutes before sun exposure. Reaooly. at least every 2 hours or after
80 minutes ofswimming or sweating.Sun Protection Measures, Spending time in the sun
increases your riskof skan cancer and early skin aging. lo decrease this risk, regularly
use asunscreen with a Broad Spectrum SPF value of 15 or higher and other
sunprotection measures including, limit time in sun, especiallv from 10 a.m.-2p.m, and
wear long-sleeved shirts, pants, hats, and sunalasses. Chitdrenunder 6 months of age:
ask a doctor.
- DOSAGE & ADMINISTRATION
- WHEN USING
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SUNSCREEN SETTING SPRITZ, SPF 45
sunscreen setting spray liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70000-1543 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 2.94 g in 60 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 5.7 g in 60 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 1.74 g in 60 mL Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL LAURATE (UNII: 668Z5835Z3) ALCOHOL (UNII: 3K9958V90M) BHT (UNII: 1P9D0Z171K) PEG-400 (UNII: B697894SGQ) AQUA (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70000-1543-1 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/15/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/15/2024 Labeler - Cardinal Health, inc. (063997360)
