GLYTONE DAILY BODY- glytone daily body lotion broad spectrum sunscreen spf 15 lotion

Glytone Daily Body by

Drug Labeling and Warnings

Glytone Daily Body by is a Otc medication manufactured, distributed, or labeled by Glytone, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Helps prevent sunburn.

DOSAGE & ADMINISTRATION

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.

PURPOSE

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

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.

INACTIVE INGREDIENT

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.

KEEP OUT OF REACH OF CHILDREN

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GLYTONE DAILY BODY 
glytone daily body lotion broad spectrum sunscreen spf 15 lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84262-027
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	2 g  in 100 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7.5 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	1.86 g  in 100 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
CARBOMER (UNII: 0A5MM307FC)
TOCOPHERSOLAN (UNII: O03S90U1F2)
FRAGRANCE 13576 (UNII: 5EM498GW35)
EDETATE DISODIUM (UNII: 7FLD91C86K)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
DIMETHICONE (UNII: 92RU3N3Y1O)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CETYL ALCOHOL (UNII: 936JST6JCN)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84262-027-01	355 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/01/2025

Labeler - Glytone, LLC (119226548)

Registrant - Glytone, LLC (119226548)