Glytone Daily Body

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
Glytone Daily Body
Generic name
GLYTONE DAILY BODY LOTION BROAD SPECTRUM SUNSCREEN SPF 15
Manufacturer
Glytone, LLC
Product type
HUMAN OTC DRUG
SPL set ID
3843ff02-2443-7780-e063-6294a90a655d
SPL ID
3843ff02-2444-7780-e063-6294a90a655d
Version
1
Effective date
2025-06-23
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 05:54:13
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 · 1 matching rows.

warnings

For external use only. Sunburn alert: This product contains an alpha hydroxy acid (AHA) that may increase your skin’s sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing, and limit sun exposure while using this product and for one week afterwards. Do not use: - on damaged or broken skin. - as a sunscreen for sunbathing. When using this product: - keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if: - rash occurs. Keep out of reach of children. Do not swallow. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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