United States · FDA National Drug Code directory
Ultra Sunscreen
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
- 85448-003_4ed974b8-6c12-08e0-e063-6294a90a7713
- Product NDC
- 85448-003
- Form
- EMULSION
- Composition / generic term
- Octinoxate, Octisalate, Titanium Dioxide
- Labeler
- Jiangsu Senwo Medical Technology Co., Ltd.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20260407
- Source listing expiry
- 20271231
Source-listed ingredients
- OCTINOXATE — .09 g/mL
- OCTISALATE — .035 g/mL
- TITANIUM DIOXIDE — .027 g/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 473 mL in 1 BOTTLE (85448-003-01) · 85448-003-01
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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