Drug labels

Halo Glow Skin Tint SPF 50 84504

ZINC OXIDE · e.l.f. Cosmetics, Inc. · TOPICAL

HUMAN OTC DRUG
Open FDA's page for this record
Set ID
223efabb-d018-c337-e063-6394a90a5605
ID
3135834f-ddd7-2cdc-e063-6394a90a6152
Effective time
20250325
Version
3
SPL product data elements

Halo Glow Skin Tint SPF 50 84504 Zinc Oxide ISODODECANE CALCIUM SODIUM BOROSILICATE BUTYLOCTYL SALICYLATE POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE LAURYL PEG-8 DIMETHICONE (300 CPS) ALUMINUM HYDROXIDE C13-15 ALKANE .BETA.-BISABOLOL SODIUM HYDROXIDE CAPRYLYL TRIMETHICONE FERRIC OXIDE YELLOW ZINC OXIDE ZINC OXIDE WATER PROPANEDIOL FERROSOFERRIC OXIDE ALKYL (C12-15) BENZOATE SILICA DIMETHYL SILYLATE DISTEARDIMONIUM HECTORITE ETHYLHEXYLGLYCERIN PHENOXYETHANOL HEXYLENE GLYCOL FERRIC OXIDE RED TRIDECYL SALICYLATE SODIUM CHLORIDE DIMETHICONE POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE TITANIUM DIOXIDE NIACINAMIDE POLYGLYCERYL-3 RICINOLEATE CAPRYLYL GLYCOL ALLANTOIN HYDROGENATED SOYBEAN LECITHIN TETRASODIUM GLUTAMATE DIACETATE OCTYLDODECYL NEOPENTANOATE LECITHIN, SOYBEAN

SPL unclassified section
Drug Facts
Active ingredient
Active Ingredients Zinc Oxide 12%
Purpose
Purpose Sunscreen
Indications and usage

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

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.

Do not use
Do not use on damaged or broken skin.
When using
When using this product keep out of eyes. Rinse with water to remove.
Stop use
Stop use and ask a doctor if: rash occurs.
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.
Dosage and administration

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 safety information
Other Information Protect the product in this container from excessive heat and direct sun.
Inactive ingredient

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
Questions or comments? 1-888-315-9814
Package label principal display panel
Packaging Label Packaging Label
Harmonized identifiers (openFDA)
Application number
M020
Brand name
Halo Glow Skin Tint SPF 50 84504
Generic name
ZINC OXIDE
Manufacturer name
e.l.f. Cosmetics, Inc.
Product NDC
76354-550
Product type
HUMAN OTC DRUG
Route
TOPICAL
Substance name
ZINC OXIDE
SPL ID
3135834f-ddd7-2cdc-e063-6394a90a6152
SPL set ID
223efabb-d018-c337-e063-6394a90a5605
Package NDC
76354-550-01
Is original packager
true
UNII
SOI2LOH54Z
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.