Ulta

1 FDA products 1 active ingredients HUMAN OTC DRUG

Ulta is listed as the manufacturer on 1 FDA drug label records covering 1 distinct active ingredients predominantly human otc drug products.

About Ulta

Ulta is named as the labeler on 1 FDA drug label records. Its catalogue spans 1 distinct active ingredients, led by AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE. Most of these labels are human otc drug products. Labelling across this portfolio most often references: helps prevent, sun protection, measures see, directions decreases, risk skin, aging caused. Use the table below to identify a specific product, then open it for full indications, dosage and warnings as filed with the FDA.

Active ingredients in this portfolio

Dosage forms and routes

Dosage formProductsRouteProducts
— — TOPICAL 1
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FDA drug products from Ulta

Brand nameGenericTypeRoute
ULTA FACE SPF 30 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE HUMAN OTC DRUG TOPICAL

Frequently asked questions

How many FDA drug products does Ulta make?
1 FDA drug label records name Ulta as the manufacturer, covering 1 distinct active ingredients.

What active ingredients does Ulta produce?
The most frequent active ingredients in this portfolio are AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE.

Are Ulta products prescription or over-the-counter?
The largest share of this company’s labels are human otc drug products; check each product page for its own marketing status.

Does this page list prices or where to buy?
No. This is a labelling reference built from FDA data. It does not sell, price or recommend any medicine.

Labelling data reproduced from FDA Structured Product Labelling for identification only. This site does not sell, price or recommend any medicine.