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
- 72288-714_4c212fda-1319-8ed8-e063-6294a90ab8fd
- Product NDC
- 72288-714
- Form
- LOTION
- Composition / generic term
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Labeler
- Amazon.com Services LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20190831
- Source listing expiry
- 20271231
Source-listed ingredients
- AVOBENZONE — 30.3 mg/mL
- HOMOSALATE — 101 mg/mL
- OCTISALATE — 50.5 mg/mL
- OCTOCRYLENE — 101 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 236 mL in 1 BOTTLE, PLASTIC (72288-714-34) · 72288-714-34
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 →