United States · FDA National Drug Code directory
H.E.B Solutions 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
- 37808-956_248a0777-7394-dea1-e063-6394a90a444a
- Product NDC
- 37808-956
- Form
- LOTION
- Composition / generic term
- Ultra SPF 50 Lotion
- Labeler
- H.E.B
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20120220
- Source listing expiry
- 20261231
Source-listed ingredients
- AVOBENZONE — 20 mg/mL
- HOMOSALATE — 100 mg/mL
- OCTISALATE — 50 mg/mL
- OCTOCRYLENE — 70 mg/mL
- OXYBENZONE — 60 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 89 mL in 1 TUBE (37808-956-09) · 37808-956-09
- 237 mL in 1 TUBE (37808-956-12) · 37808-956-12
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 →