FDA label 4ce8d76f-c12b-678b-e063-6294a90a3d42

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
95871f35-3413-43c2-9745-7913b84ef215
SPL ID
4ce8d76f-c12b-678b-e063-6294a90a3d42
Version
10
Effective date
2026-03-13
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:12:33

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 May stain or damage some fabrics or surfaces DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202 *COPPERTONE ® AND COPPERTONE ULTRA GUARD ® ARE REGISTERED TRADEMARKS OF BEIERSDORF AG. BEIERSDORF IS NOT AFFILATED 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.