H.E.B ULTRA

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
H.E.B ULTRA
Generic name
SPF 30 SUNSCREEN
Manufacturer
H.E.B
Product type
HUMAN OTC DRUG
SPL set ID
90287874-cdfa-489c-936d-e487f6b3db96
SPL ID
c71836b9-92d1-6659-e053-2a95a90aa3a5
Version
2
Effective date
2024-10-15
Source export date
2026-10-30
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:26:41
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings For external use only

warnings and cautions

FLAMMABLE: do not use near heat, flame or while smoking avoid long term storage above 104°F (40°C)

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.