Quick answers
- What is Benzoin resin used for?
- The Drug Facts label of Benzoin Compound Tincture (Humco Holding Group, Inc.) lists these uses: Forms a coating over wound for protecting recurring canker sores.
- Do I need a prescription for Benzoin resin?
- No. The products on this page are sold without a prescription (over the counter).
- Is a store brand the same as the name brand?
- Products listed together below have the same active ingredient, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
- Has Benzoin resin been recalled?
- No recall linked to these products appears in the FDA enforcement reports we use.
Drug Facts label
Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.
Benzoin Compound Tincture · Humco Holding Group, Inc.
Benzoin resin 1000 mg/mL, liquid (topical)
Active ingredient
Benzoin
Purpose
Oral mucosal protectant
Uses
Forms a coating over wound for protecting recurring canker sores
Warnings
For external use only. Do not swallow. Do not exceed recommended dosage.
When using this product
Children under 12 years of age should be supervised in the use of this product.
Do not use
for more than 7 days unless directed by a dentist or doctor. Stop use and consult a dentist or doctor if sore mouth symptoms do not improve in 7 days. irritation, pain or redness persists or worsens. swelling, rash or fever develops.
Keep out of reach of children
In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.
Directions
Adults and children 6 months of age and older: Dry the affected area, with cotton swab, apply undiluted to the affected area not more often than every 2 hours. Children under 6 months of age: Consult a dentist or doctor.
Other information
- Flammable: Keep away from spark, heat or flame.
Inactive ingredients
Alcohol 77%, Aloe, Storax, Tolu Balsam
— FDA label of Benzoin Compound Tincture, Humco Holding Group, Inc., effective December 11, 2025. See the official label on DailyMed →
Compound Benzoin Tincture · Medical Chemical Corporation
Benzoin resin 10%, liquid (topical)
Active ingredient
Aloe, Benzoin, Storax, Tolu Balsam, Ethanol
Purpose
Antiseptic
Uses
Directions: Apply to affected area for first-aid treatment of minor cuts and abrasions. Discontinue use and get medical aid if redness, irritation or infection develops. In case of deep or puncture wounds consult a physician.
Warnings
Keep out of reach of children
Ingestion will result in a severe gastrointestinal distress, unconsciousness and death. If ingested induce vomiting if victim is conscious. Contact a poison control center immediately. Warnings:
Keep out of reach of children
Ingestion will result in severe gastrointestinal distress, unconsciousness and death. If ingested induce vomiting if the victim is conscious. Contact a poison control center immediately.
Directions
Apply to affected area for first-aid treatment of minor cuts and abrasions. Discontinue use and get medical aid if redness, irritation or infection develops. In case of deep or puncture wounds consult a physician.
Inactive ingredients
Enter section text here
— FDA label of Compound Benzoin Tincture, Medical Chemical Corporation, effective July 1, 2026. See the official label on DailyMed →
This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.
Same medicine, other brands
Each group lists the products that have exactly the same active ingredient, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.
Benzoin resin 1000 mg/mL · liquid (topical) · 5 products
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Benzoin Compound Tincture | Humco Holding Group, Inc. | DailyMed |
| Benzoin Tincture | 116956644 | DailyMed |
| Benzoin Tincture | Humco Holding Group, Inc. | DailyMed |
| Benzoin Tincture | Pharma Nobis, LLC | DailyMed |
| Sunmark Benzoin Compound Tincture | Strategic Sourcing Services LLC | DailyMed |
Benzoin resin 10% · liquid (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Compound Benzoin Tincture | Medical Chemical Corporation | DailyMed |
Companies that sell this medicine
The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.
- Humco Holding Group, Inc.2 products
- Medical Chemical Corporation1 product
- 1169566441 product
- Pharma Nobis, LLC1 product
- Strategic Sourcing Services LLC1 product
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- FDA rule for the Drug Facts label (21 CFR 201.66)
Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.