FDA.reportPublic FDA data

Oars & Alps SPF 30 100% Mineral Antioxidant Sunscreen Spray

Manufacturer
Oars and Alps LLC
Effective date
2022-11-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:49:06

Label at a glance#

ProductOars and Alps 100% Mineral Antioxidant Sunscreen
Active ingredientZINC OXIDE
Label structure10 sections

Indications and uses

Helps prevent sunburn If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Dosage and administration

Apply generously and evenly 15 minutes before sun exposure. Hold container 4-6 inches from the skin to apply. Do not spray directly into the face. Spray onto hands and rub into face. Do not inhale. Do not apply in windy conditions Use in well-ventilated area 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 ...

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide - 15.0%

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn
  • If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

WARNINGS SECTION

• For external use only.

• Flammable. Contents under pressure. Keep away from fire, smoke, other sources of ignition or while smoking. Do not puncture of incinerate can. Do not store above 120 F.
• 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply generously and evenly 15 minutes before sun exposure.
  • Hold container 4-6 inches from the skin to apply.
  • Do not spray directly into the face. Spray onto hands and rub into face. Do not inhale.
  • Do not apply in windy conditions
  • Use in well-ventilated area
  • 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 a.m. – 2 p.m. • Wear long-sleeved shirts, pants, hats, and sunglasses.​

Children under six months: Ask a doctor.

INACTIVE INGREDIENT SECTION

Bentonite, Bisabolol, Butyloctyl Salicylate, C12-15 Alkyl Benzoate, Caprylhydroxamic Acid, Caprylyl Glycol, Cellulose Gum, Cetearyl Alcohol, Citric Acid, Cladonia Stellaris Extract, Coco-Glucoside, Fructose, Glycerin, Helianthus Annuus (Sunflower) Seed Oil, Microcrystalline Cellulose, Octyldodecyl Neopentanoate, PPG-12/SMDI Copolymer, Propanediol, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium Gluconate, Sodium Stearoyl Glutamate, Tocopheryl Acetate, Water, Withania Somnifera Root Extract, Xanthan Gum

OTHER SAFETY INFORMATION

Protect this product in this container from excessive heat and direct sun.

OTC - QUESTIONS SECTION

Contact Hi@oarsandalps.com (630) 635-7839

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83046-37283046-372-13

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
PPG-12/SMDI COPOLYMER1BK9DDD24EIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
CLADONIA RANGIFERINA WHOLEO21ZF987XQIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
COCO GLUCOSIDEICS790225BIACT
JOJOBA OIL724GKU717MIACT
SODIUM GLUCONATER6Q3791S76IACT
SODIUM STEAROYL GLUTAMATE65A9F4P024IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WITHANIA SOMNIFERA ROOTV038D626IFIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
PROPANEDIOL5965N8W85TIACT
WATER059QF0KO0RIACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIEDK679OBS311IACT
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
FRUCTOSE6YSS42VSEVIACT
ZINC OXIDESOI2LOH54ZACTIB
LEVOMENOL24WE03BX2TIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
CAPRYLYL GLYCOL00YIU5438UIACT
XANTHAN GUMTTV12P4NEEIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
GLYCERINPDC6A3C0OXIACT
SUNFLOWER OIL3W1JG795YIIACT
BENTONITEA3N5ZCN45CIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ed11680d-5476-8fb4-e053-2a95a90a96e2ed11680d-5475-8fb4-e053-2a95a90a96e22022-11-09WarningsExact identifier
spl id: ed11680d-5476-8fb4-e053-2a95a90a96e2
spl set id: ed11680d-5475-8fb4-e053-2a95a90a96e2

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.