Zinc Oxide

SKIN PROTECTANT TOPICAL HUMAN OTC DRUG

Zinc Oxide is an FDA drug label for the active ingredient SKIN PROTECTANT manufactured by BluePoint Laboratories 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 20231117.

Generic name
SKIN PROTECTANT
Manufacturer
BluePoint Laboratories
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
68001-532
Application
M016
Label effective
20231117

Active ingredients

Active Ingredient Zinc Oxide 20% w/w

Indications & Usage

Uses • Dries the oozing and weeping of poison: • Ivy • Oak • Sumac

Dosage & Administration

Directions For poison ivy, oak, and sumac: apply as needed.

Contraindications

Not available.

Warnings

Warnings For External Use Only When using this product • Do not get into eyes • Do not use over large areas of the body Stop use and ask a doctor if • The condition worsens • Symptoms last more than 7 days or clear up and occur again within a few days • You are allergic to any of these ingredients Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.

Adverse Reactions

Not available.