Cuadriderma
Cuadriderma is an FDA drug label for the active ingredient BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE manufactured by ProMex LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20220125.
- Generic name
- BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE
- Manufacturer
- ProMex LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 58988-1170
- Application
- M004
- Label effective
- 20220125
Active ingredients
Indications & Usage
Uses helps prevent infection in and temporarily relieves pain due to * minor cuts * scrapes * burns
Dosage & Administration
Directions Adults and children 2 years and older: * clean affected area * apply a small amount (equal to surface area of tip of finger) on area 1 to 3 times daily. * may be covered with sterile bandage. Children under 2 years: ask a doctor
Contraindications
Not available.
Warnings
Warnings For external use only Allergy alert * do not use if allergic to any of the ingredients Do not use * in or near the eyes * on large areas of the body Ask a doctor before use if you have * deep or puncture wounds * animal bites * serious burns When using this product * do not use longer than 1 week Stop use and ask a doctor if * condition lasts or gets worse * symptoms last for more than 7 days or clear up and come back within a few days * a rash or other allergic reaction occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Adverse Reactions
Not available.