FDA label 40063239-1043-629f-e063-6394a90a36f9

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)

SPL set ID
e47872ad-01a4-45f0-9399-4f7abc4e5ca3
SPL ID
40063239-1043-629f-e063-6394a90a36f9
Version
10
Effective date
2025-09-30
Source export date
2026-11-06
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/423686b2ac39507df6931677ae004637f2f017f82cbe44b047a75ba358b9d453/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run
20261106T075659Z
Imported at
2026-11-06 08:58:33

Warnings cross-check#

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

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only

Adverse reactions cross-check#

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

Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

ADVERSE REACTION DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202 MAY STAIN OR DAMAGE SOME FABRICS OR SURFACES. *Neutrogena and ultra sheer are registered trademarks of Johnson & Johnson Corporation, New Brunswick, NJ 09933. Johnson & Johnson Corporation is not affiliated with the Kroger Co. or this product. **OXYBENZONE & OCTINOXATE FREE Quality guarantee 800-632-6900 www.kroger.com

Reported adverse events (FAERS/openFDA)#

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