UP & UP

2 FDA products 2 active ingredients HUMAN OTC DRUG

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

About UP & UP

UP & UP is named as the labeler on 2 FDA drug label records. Its catalogue spans 2 distinct active ingredients, led by LORATADINE, OMEPRAZOLE MAGNESIUM. Most of these labels are human otc drug products. Labelling across this portfolio most often references: treats frequent, heartburn occurs, days week, immediate relief, full effect, temporarily relieves, symptoms due, hay fever. 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

Active ingredientProducts
LORATADINE 1
OMEPRAZOLE MAGNESIUM 1

Dosage forms and routes

Dosage formProductsRouteProducts
— — ORAL 2
— — — —
— — — —
— — — —
— — — —
— — — —

FDA drug products from UP & UP

Brand nameGenericTypeRoute
DYE-FREE CHILDRENS LORATADINE LORATADINE HUMAN OTC DRUG ORAL
Omeprazole OMEPRAZOLE MAGNESIUM HUMAN OTC DRUG ORAL

Frequently asked questions

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

What active ingredients does UP & UP produce?
The most frequent active ingredients in this portfolio are LORATADINE, OMEPRAZOLE MAGNESIUM.

Are UP & UP 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.