HALO GLOW SKIN TINT SPF50 -84518- zinc oxide lotion

Halo Glow Skin Tint SPF50 -84518 by

Drug Labeling and Warnings

Halo Glow Skin Tint SPF50 -84518 by is a Otc medication manufactured, distributed, or labeled by e.l.f. Cosmetics, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Zinc Oxide 12%

Purpose

Sunscreen

Uses

• Helps prevent sunburn
• If used as directed with other sun protection measures (see Directions) decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

For external use only.

Do not use

on damaged or broken skin.

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

• If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Apply generously and evenly 15 minutes before sun exposure.
• Reapply after 80 minutes of swimming or sweating.
• immediately after towel drying.
• at least every 2 hours.
• Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
• Limit time in sun, especially from 10 a.m.-2 p.m.
• Wear long-sleeved shirts, pants, hats and sunglasses.
• Children under 6 months: Ask a doctor.

Other information

• Protect the product in this container from excessive heat and direct sun.

Inactive ingredients

Water, C12-15 Alkyl Benzoate, Lauryl PEG-8 Dimethicone, Tridecyl Salicylate, Isododecane, Propanediol, Butyloctyl Salicylate, Calcium Sodium Borosilicate, Dimethicone, Niacinamide, C13-15 Alkane, Caprylyl Methicone, Silica, Polyglyceryl-2 Dipolyhydroxystearate, Polyglyceryl-3 Polyricinoleate, Sodium Chloride, Octyldodecyl Neopentanoate, Disteardimonium Hectorite, Phenoxyethanol, Bisabolol, Lecithin, Caprylyl Glycol, Allantoin, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Hydrogenated Lecithin, Ethylhexylglycerin, Hexylene Glycol, Tetrasodium Glutamate Diacetate, Sodium Hydroxide

May Contain: Iron Oxides (CI 77491, CI 77492, CI 77499)

Package Label

INGREDIENTS AND APPEARANCE

HALO GLOW SKIN TINT SPF50 -84518 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76354-664
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	120 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
FERRIC OXIDE RED (UNII: 1K09F3G675)
ISODODECANE (UNII: A8289P68Y2)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
CALCIUM SODIUM BOROSILICATE (UNII: 4MM76N4WMY)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
ALLANTOIN (UNII: 344S277G0Z)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
LAURYL PEG-8 DIMETHICONE (300 CPS) (UNII: ELL2U7K8T8)
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
CAPRYLYL METHICONE (UNII: Q95M2P1KJL)
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)
DIMETHICONE (UNII: 92RU3N3Y1O)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
SILICA (UNII: ETJ7Z6XBU4)
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
NIACINAMIDE (UNII: 25X51I8RD4)
C13-15 ALKANE (UNII: 114P5I43UJ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
WATER (UNII: 059QF0KO0R)
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)
PROPANEDIOL (UNII: 5965N8W85T)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
BISABOLOL (UNII: 24WE03BX2T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76354-664-01	1 in 1 CARTON	05/05/2025
1		30 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	05/05/2025

Labeler - e.l.f. Cosmetics, Inc. (093902816)