Glytone Daily Body

Manufacturer
Glytone, LLC
Effective date
2025-06-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:07:01

Label at a glance#

ProductGlytone Daily Body
Active ingredientAVOBENZONE, OCTINOXATE, OCTOCRYLENE, OXYBENZONE
Label structure8 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Helps prevent sunburn.

DOSAGE & ADMINISTRATION SECTION

Apply Daily Body Lotion once daily or as directed by a doctor at least 15 minutes before sun exposure.
Reapply at least every 2 hours. Use a water resistant sunscreen if swimming or sweating.

OTC - PURPOSE SECTION

Avobenzone 2% – Sunscreen
Octinoxate 7.5% – Sunscreen
Octocrylene 1.86% – Sunscreen
Oxybenzone 3% – Sunscreen

WARNINGS SECTION

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.

INACTIVE INGREDIENT SECTION

Water, Glycolic Acid, C12-15 Alkyl Benzoate, Cyclopentasiloxane, Sodium Hydroxide, Glycerin, Glyceryl Stearate, PEG-100 Stearate, Cetearyl Alcohol, Cyclotetrasiloxane, PEG-40 Stearate, Butyrospermum Parkii (Shea) Butter, C13-14 Isoparaffin, Cetearyl Glucoside, Cetyl Alcohol, Cholesterol, Dimethiconol, Disodium EDTA, Laureth-7, Methylparaben, Phenoxyethanol, Polyacrylamide, Tocopheryl Acetate, Xanthan Gum.

RECENT MAJOR CHANGES SECTION

deleted undefined photo

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84262-027-01Glytone Daily Body355 g in 1 BOTTLE, PUMPLOTION3551

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84262-02784262-027-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Glytone Daily BodyGLYTONE DAILY BODY LOTION BROAD SPECTRUM SUNSCREEN SPF 15Glytone, LLC3843ff02-2443-7780-e063-6294a90a655d2025-06-23WarningsExact identifier
ndc (package): 84262-027-01
ndc (product): 84262-027
ndc11 (package): 84262002701
spl id: 3843ff02-2444-7780-e063-6294a90a655d
spl set id: 3843ff02-2443-7780-e063-6294a90a655d

Reported adverse events (FAERS/openFDA)#

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