United States · FDA National Drug Code directory
Arizona Sun Sunscreen SPF 8
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 61973-100_4f0c8f3f-68e2-8c30-e063-6394a90a6805
- Product NDC
- 61973-100
- Form
- LOTION
- Composition / generic term
- Sunscreen
- Labeler
- Arizona Sun Products
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20240202
- Source listing expiry
- 20271231
Source-listed ingredients
- OCTISALATE — 10 mg/g
- OXYBENZONE — 10 mg/g
- OCTINOXATE — 65 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 120 g in 1 BOTTLE (61973-100-04) · 61973-100-04
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →