FDA label 4ce8bdd4-38e6-0db0-e063-6294a90ac437

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
8232c887-5a20-4402-af2a-3d427c8437a2
SPL ID
4ce8bdd4-38e6-0db0-e063-6294a90ac437
Version
11
Effective date
2026-03-13
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:57:03

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#

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

adverse reactions

ADVERSE REACTION Distributed by the Kroger Co. Cincinnati, Ohio 45202 *Coppertone ® and Coppertone Ultra Guard ® are registered trademarks of Bayer, Whippany, NJ 07981, Bayer is not affliated with the Kroger Co. or this product. May stain or damage some fabrics or surfaces. **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.