HALO GLOW SKIN TINT SPF 50 84514- zinc oxide lotion

Halo Glow Skin Tint SPF 50 84514 by

Drug Labeling and Warnings

Halo Glow Skin Tint SPF 50 84514 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, Isododecane, Lauryl PEG-8 Dimethicone, Tridecyl Salicylate, Calcium Sodium Borosilicate, Propanediol, Butyloctyl Salicylate, Caprylyl Methicone, Dimethicone, Niacinamide, C13-15 Alkane, Silica, Octyldodecyl Neopentanoate, Polyglyceryl-2 Dipolyhydroxystearate, Polyglyceryl-3 Polyricinoleate, Sodium Chloride, Disteardimonium Hectorite, Phenoxyethanol, Bisabolol, Lecithin, Caprylyl Glycol, Allantoin, Aluminum Hydroxide, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Ethylhexylglycerin, Hexylene Glycol, Hydrogenated Lecithin, Tetrasodium Glutamate Diacetate, Sodium Hydroxide

May Contain:Titanium Dioxide (CI 77891), Iron Oxides (CI 77491, CI 77492, CI 77499)

Questions or comments?

1-888-315-9814

Packaging Label

INGREDIENTS AND APPEARANCE

HALO GLOW SKIN TINT SPF 50 84514 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76354-560
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
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
FERRIC OXIDE RED (UNII: 1K09F3G675)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
DIMETHICONE (UNII: 92RU3N3Y1O)
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
NIACINAMIDE (UNII: 25X51I8RD4)
POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ALLANTOIN (UNII: 344S277G0Z)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
ISODODECANE (UNII: A8289P68Y2)
CALCIUM SODIUM BOROSILICATE (UNII: 4MM76N4WMY)
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)
PROPANEDIOL (UNII: 5965N8W85T)
LAURYL PEG-8 DIMETHICONE (300 CPS) (UNII: ELL2U7K8T8)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
C13-15 ALKANE (UNII: 114P5I43UJ)
.BETA.-BISABOLOL (UNII: LP618AV2EA)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CAPRYLYL TRIMETHICONE (UNII: H6HK6E4EB1)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76354-560-01	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)