Supergoop LLC

2 FDA products 2 active ingredients HUMAN OTC DRUG

Supergoop LLC is listed as the manufacturer on 2 FDA drug label records covering 2 distinct active ingredients predominantly human otc drug products.

About Supergoop LLC

Supergoop LLC is named as the labeler on 2 FDA drug label records. Its catalogue spans 2 distinct active ingredients, led by OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE, ZINC OXIDE. Most of these labels are human otc drug products. Labelling across this portfolio most often references: ask doctor, rash occurs. 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 2
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FDA drug products from Supergoop LLC

Brand nameGenericTypeRoute
Mineral Glowscreen Soft-Radiance Drops Golden Hour ZINC OXIDE HUMAN OTC DRUG TOPICAL
Unseen Sunscreen SPF 50 OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE HUMAN OTC DRUG TOPICAL

Frequently asked questions

How many FDA drug products does Supergoop LLC make?
2 FDA drug label records name Supergoop LLC as the manufacturer, covering 2 distinct active ingredients.

What active ingredients does Supergoop LLC produce?
The most frequent active ingredients in this portfolio are OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE, ZINC OXIDE.

Are Supergoop LLC 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.