ULTRA SOOTHER DRY-TOUCH SUNSCREEN

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
ULTRA SOOTHER DRY-TOUCH SUNSCREEN
Generic name
HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE
Manufacturer
skinnplus
Product type
HUMAN OTC DRUG
SPL set ID
4dbc1035-c41c-308c-e063-6394a90a36c4
SPL ID
4dbc1035-c41d-308c-e063-6394a90a36c4
Version
1
Effective date
2026-03-23
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:28:10
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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warnings

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Reported adverse events (FAERS/openFDA)#

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