Benzoin Tincture Liquid
FDA Label NDC 70677-1200

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by 116956644 for the product Benzoin Tincture (NDC 70677-1200). 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 other, active ingredient, purpose, use, warnings, when using this product, stop use and consult a dentist or doctor if, keep out of the reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

Drug Facts

Active Ingredient

Benzoin Tincture

Purpose

Oral mucosal protectant

Use

Forms a coating over wound for protecting recurring canker sores

Warnings

For externl use only. Do not swallow. Do not exceed recommended dosage.

When Using This Product

do not use in the eyes

do not use this product for longer than 1 week unless directed by a dentist or doctor

Stop Use And Consult A Dentist Or Doctor If

  • the condition persists or gets worse
  • symptoms do not improve in 7 days.
  • pain, irritation, swelling, redness, rash or fever develop

Keep Out Of The Reach Of Children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immeditely. (1-800-222-1222)

Directions

Adult and children 6 months of age and older: Dry the affected area. Saturate a cotton applicator with medication and apply undiluted to the affected area not more than every 2 hours.

Children under 6 months of age: Consult a dentist or doctor.

Inactive Ingredients

Alcohol 79%, Aloe, Stoax, Tolu Balsam.

Questions?

Call 833-358-6431

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