Sunmark Benzoin Compound Tincture
Benzoin Resin · Liquid · Topical
Active ingredient
Active Ingredient Benzoin
Purpose
Purpose Protectant
Uses
Use Forms a coating over wound for protecting recurring canker sores
Warnings
Warnings For external use only. Do not swallow. Do not exceed recommended dosage.
When using this product
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 ask a 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
Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.
Directions
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 dentiest or doctor.
Inactive ingredients
Inactive Ingredients Alcohol 77%, Aloe, Storax, Tolu Balsam
Label text from the FDA structured product label by Strategic Sourcing Services LLC (revised Dec 19, 2023). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Benzoin Resin in 1 product
Sunmark Benzoin Compound Tincture NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 49348-138 | Benzoin Resin 1000 mg/mL Liquid | Strategic Sourcing Services LLC | OTC MONOGRAPH DRUG |
Frequently asked questions
What is Sunmark Benzoin Compound Tincture used for?
Use Forms a coating over wound for protecting recurring canker sores
Who makes Sunmark Benzoin Compound Tincture?
Sunmark Benzoin Compound Tincture is listed by 1 labeler in the FDA NDC directory, including Strategic Sourcing Services LLC.