United States · FDA National Drug Code directory
Bondi Sands SPF 60 Sunny Face
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
- 79950-019_24c78897-3137-f24b-e063-6394a90aa80a
- Product NDC
- 79950-019
- Form
- LOTION
- Composition / generic term
- AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
- Labeler
- BONDI SANDS (USA) INC.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20250108
- Source listing expiry
- 20261231
Source-listed ingredients
- AVOBENZONE — 30 mg/mL
- OCTISALATE — 50 mg/mL
- OCTOCRYLENE — 100 mg/mL
- HOMOSALATE — 150 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (79950-019-01) / 50 mL in 1 TUBE · 79950-019-01
Source and coverage
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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.
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