United States · FDA National Drug Code directory
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
- 61010-6103_10dfe53b-4cdd-c203-e063-6294a90af360
- Product NDC
- 61010-6103
- Form
- LOTION
- Composition / generic term
- Homosalate, Octinoxate, Octisalate, Oxybenzone
- Labeler
- Safetec of America, Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20070313
- Source listing expiry
- 20261231
Source-listed ingredients
- HOMOSALATE — 6 mg/g
- OCTINOXATE — 7.5 mg/g
- OCTISALATE — 5 mg/g
- OXYBENZONE — 5 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 25 PACKET in 1 BOX (61010-6103-1) / 3.5 g in 1 PACKET (61010-6103-0) · 61010-6103-1
- 25 PACKET in 1 BOX (61010-6103-3) / 2 g in 1 PACKET (61010-6103-2) · 61010-6103-3
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 →