Indications and uses
First aid to help prevent infection and provide temporary relief of pain or discomfort in minor cuts scrapes burns
Triple Antibiotic Plus Pain Relief
- Manufacturer
- Kareway Product, Inc.
- Effective date
- 2023-02-17
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:36:27
Label at a glance#
ProductTriple Antibiotic Plus Pain Relief
Active ingredientNEOMYCIN SULFATE, PRAMOXINE HYDROCHLORIDE, BACITRACIN ZINC, POLYMYXIN B SULFATE
Label structure7 sections
Dosage and administration
adults and children 2 years of age and older: clean the affected area apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily may be covered with a sterile bandage children under 2 years of age: consult a physician
Storage and handling
store at 20°-25°C (68°-77°F)
Label contents#
Full prescribing information#
Active Ingredients (in each gram)
Bacitracin Zinc 500units
Neomycin 3.5mg
Polymyxin B Sulfate 10,000 units
Pramoxine HCl 10mg
Purpose
| Active ingredients
(each gram contains) | Purpose |
|---|---|
| Bacitracin zinc 500 units | First aid antibiotic |
| Neomycin sulfate 3.5 mg | First aid antibiotic |
| Polymyxin B sulfate 10,000 units | First aid antibiotic |
| Pramoxine HCI 10 mg | External analgesic |
Uses
First aid to help prevent infection and provide temporary relief of pain or discomfort in minor
- cuts
- scrapes
- burns
Warnings
For external use only
Do not use
- if you are allergic to any of the ingredients
- in the eyes
- over large areas of the body
Ask a doctor before use if you have
Ask a doctor before use if you have
- deep or puncture wounds
- animal bites
- serious burns
Stop use and ask a doctor if
- you need to use longer than 1 week
- condition persists or gets worse
- condition persists for more than 1 week, or clear up and occur again within a few days
- a rash or other allergic reaction develops
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Other information
store at 20°-25°C (68°-77°F)
Directions
adults and children 2 years of age and older:
- clean the affected area
- apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily
- may be covered with a sterile bandage
children under 2 years of age: consult a physician
Inactive ingredients
white petrolatum
PRINCIPAL DISPLAY PANEL
Triple Antibiotic Ointment + Pain Relief
Bacitracin Zinc • Neomycin Sulfate • Polymyxin B Sulfate • Pramoxine HCl
First Aid Antibiotic Ointment
Maximum Strength
NET WT 1 oz (28.3 g)
FDA-Initiated Inactive NDC Indexing#
Products#
Every source-derived product name is available through these pages.
- Triple Antibiotic Plus Pain Relief
- Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride
- PETROLATUM
- NEOMYCIN SULFATE
- NEOMYCIN
- PRAMOXINE HYDROCHLORIDE
- PRAMOXINE
- BACITRACIN ZINC
- BACITRACIN
- POLYMYXIN B SULFATE
- POLYMYXIN B
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 67510-1670 | 67510-1670-3, 67510-1670-1, 67510-1670-5 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| PETROLATUM | 4T6H12BN9U | IACT |
| NEOMYCIN SULFATE | 057Y626693 | ACTIB |
| PRAMOXINE HYDROCHLORIDE | 88AYB867L5 | ACTIB |
| BACITRACIN ZINC | 89Y4M234ES | ACTIM |
| POLYMYXIN B SULFATE | 19371312D4 | ACTIM |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| f4ee870c-a1dc-1d42-e053-2a95a90ada2d | 5542da3f-595f-0612-e054-00144ff8d46c | 2023-02-17 | Warnings | f4ee870c-a1dc-1d42-e053-2a95a90ada2d 5542da3f-595f-0612-e054-00144ff8d46c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.