HALO GLOW SKIN TINT SPF50-84505- zinc oxide lotion

Halo Glow Skin Tint SPF50-84505 by

Drug Labeling and Warnings

Halo Glow Skin Tint SPF50-84505 by is a Otc medication manufactured, distributed, or labeled by e.l.f. Cosmetics, Inc., Nanophase Technologies Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

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

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, Aluminum Hydroxide, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Hydrogenated Lecithin, Ethylhexylglycerin, Hexylene Glycol, Tetrasodium Glutamate Diacetate, Sodium Hydroxide

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

Questions or comments?

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Package Label

INGREDIENTS AND APPEARANCE

HALO GLOW SKIN TINT SPF50-84505 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76354-551
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 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ISODODECANE (UNII: A8289P68Y2)
CAPRYLYL METHICONE (UNII: Q95M2P1KJL)
BISABOLOL (UNII: 24WE03BX2T)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PROPANEDIOL (UNII: 5965N8W85T)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
WATER (UNII: 059QF0KO0R)
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
LAURYL PEG-8 DIMETHICONE (300 CPS) (UNII: ELL2U7K8T8)
C13-15 ALKANE (UNII: 114P5I43UJ)
SILICA (UNII: ETJ7Z6XBU4)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
ALLANTOIN (UNII: 344S277G0Z)
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
NIACINAMIDE (UNII: 25X51I8RD4)
POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
DIMETHICONE (UNII: 92RU3N3Y1O)
FERRIC OXIDE RED (UNII: 1K09F3G675)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
CALCIUM SODIUM BOROSILICATE (UNII: 4MM76N4WMY)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76354-551-01	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)

Establishment
Name	Address	ID/FEI	Business Operations
Nanophase Technologies Corporation		118812921	manufacture(76354-551)