Active Ingredients
Phenol, 1.5%
Zinc Oxide, 6.6%
Unguentine Ointment
FDA Label NDC 45728-446
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Oakhurst Company for the product Unguentine (NDC 45728-446). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, ask a doctor before use if you have, when using this product, stop use and ask a docter if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
First Aid Antiseptic
Skin Protectant
Uses
First aid for the temporary protection of minor cuts, scrapes, and burns.
Warnings
For external use only
Ask A Doctor Before Use If You Have
- deep or puncture wounds, animal bites or serious burns
When Using This Product
- Do not get into eyes
- Do not apply to large areas of body
- Do not bandage
- Do not exceed recommended dosage
Stop Use And Ask A Docter If
- the condition persists or gets worse
- the condition does not improve within 7 days
Keep Out Of Reach Of Children
- In case of accidental ingestion, seel professional assistance or contact a Poison Control Center immediately.
Directions
- Clean affected area
- Apply a small amount to the affected area 1 to 3 times daily
Other Information
- Keep container closed when not in use
- Store at 59°F to 86°F (15° to 30°C)
Inactive Ingredients
Camphor, Lavender Oil, Petrolatum
Question Or Comments
- 1-800-831-1135, visit our website at www.oakhurstco.com
Package Label.Principal Display Panel
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