Caring Mill Triple Antibiotic and Pain PRAMOXINE HYDROCHLORIDE, BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE 10 mg/g; 500 [USP'U]/g; 10000 [USP'U]/g; 3.5 mg/g Ointment, 1 tube — NDC 81522-050-01 (Billing 81522-0050-01)
This is a package of 1 tube of Caring Mill Triple Antibiotic and Pain PRAMOXINE HYDROCHLORIDE, BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE 10 mg/g; 500 [USP'U]/g; 10000 [USP'U]/g; 3.5 mg/g Ointment from FSA Store Inc. (Caring Mills), marketed since Oct 2025 and currently FDA-listed. It is this product's only package size.
NDC database record
One package, one record: these facts belong to NDC 81522-050-01 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 81522 labeler · 050 product · 01 package
- Package marketed since
- Oct 1, 2025
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2026
- Barcode (UPC-A, from the NDC)
- 3 8152205001 9
- FDA record last changed
- Aug 27, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
- RxCUI (RxNorm): 1359350
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 8, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 8, 2026
RxNorm drug class
This medicine belongs to the Other antibiotics for topical use class.
Where does this data come from?
- RxClass (NLM) · catalog refreshed Oct 8, 2026
Clinical
Neomycin, polymyxin, and bacitracin combination is used to prevent minor skin injuries such as cuts, scrapes, and burns from becoming infected. Neomycin, polymyxin, and bacitracin are in a class of medications called antibiotics. Neomycin, polymyxin, and bacitracin combination works by stopping the growth of bacteria.
Read the full MedlinePlus article ↗Caring Mill Triple Antibiotic and Pain is a topical ointment containing three antibiotics (bacitracin, neomycin, and polymyxin B) and a local anesthetic (pramoxine). The antibiotics are typically used to help prevent bacterial infection in minor cuts, scrapes, and wounds. Pramoxine functions as a numbing agent commonly used to reduce pain and itching in topical products. This is an over-the-counter monograph drug, meaning it is marketed under FDA's established category rules rather than as an individually reviewed product.
Patient education
Supplement & herbal interactions
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
Ask a licensed pharmacist directly — free, answered by our team.
Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per g | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
Where does this data come from?
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 9, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 81522-0050-01 You're viewing this Main listing | 1 TUBE in 1 PACKAGE / 28.3 g in 1 TUBE | 2025-10-01 | — | Active |
Therapeutic equivalents
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
- FDA Orange Book · refreshed Oct 3, 2026
Inactive Ingredients / Excipients
Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
UNII B6E5W8RQJ4
White petrolatum is a purified mineral oil product used as a lubricant and skin protectant in medications. It helps pills slide through manufacturing equipment and can soften or protect the skin when applied topically.
1 inactive ingredient listed in the exact product block matched to this NDC.
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.- FDA label on DailyMed · label index refreshed Oct 8, 2026
- FDA openFDA NDC Directory · synced Oct 8, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
Why might an inactive ingredient be missing?
Can inactive ingredients matter?
Manufacturer & labeler
More NDCs from FSA Store Inc. (Caring Mills) labeler code 81522
- Aspirin 325 mg Tablet, Coated NDC 81522-018-11
- Naproxen Sodium 220 mg Tablet, Coated NDC 81522-045-05
- Tolnaftate Antifungal Spray Liquid 10 mg/g Aerosol, Spray NDC 81522-068-01
- Menthol Maximum Strength Medicated Foot Powder Talc Free 10 mg/g Powder NDC 81522-069-01
- Acetaminophen Extra Strength 500 mg Tablet, Coated NDC 81522-070-13
- Wart Removers Salicylic Acid .4 g/g Patch NDC 81522-076-01
- Maximum Strength Antifungal Liquid Tolnaftate 10 mg/mL Liquid NDC 81522-077-01
- Acetaminophen PM Acetaminophen and Diphenhydramine Hydrochloride 500 mg; 25 mg Tablet, Coated NDC 81522-095-03
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Uses First aid to prevent infection and for the temporary relief of pain in minor: ■ cuts ■ scrapes ■ burns
⏱️ Dosage and Administration ▾
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 finnger) on the area 1 to 3 times daily ■ may be covered with a sterile bandage Children under 2 years of age ■ do not use, ask a doctor
⚠️ Warnings ▾
Warnings For External use only
🧪 Active Ingredient ▾
Active Ingredient 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 HCl (10 mg)........................ Topical analgesic
🧪 Inactive Ingredients ▾
Inactive Ingredient white petrolatum
🎯 Purpose ▾
Purpose First aid antibiotic First aid antibiotic First aid antibiotic Topical analgesic
📄 Do Not Use ▾
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 ▾
Ask a doctor before use if you have ■ deep or puncture wounds ■ serious burns ■ animal bites
📄 When Using This Product ▾
When using this product ■ use only as directed
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor if ■ you need to use longer than 1 week ■ condition persists or gets worse ■ symptoms persist for more than 7 days or clear up and occur again within a few days ■ rash or other allergic reaction develops
📄 Keep Out of Reach of Children ▾
Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
📄 Other Information ▾
Other information ■ store at 20º-25ºC (68º-77ºF) ■ do not use if tube seal under cap is broken
📄 Questions or Comments ▾
Questions or Comment? Call 1-866-326-1313
📄 Package Label / Principal Display Panel ▾
Label label
About this NDC listing & data coverage
What data is (and isn’t) available for this NDC — tap to expand
| NDC identity (package / product / labeler codes) | ✓ Available |
| Labeler | ✓ Available |
| Product & package description | ✓ Available |
| Marketing category & status | ✓ Available |
| Active ingredient / dosage form / route | ✓ Available |
| FDA label (SPL via DailyMed) | ✓ Available |
| Package photos | ✓ Available |
| Inactive ingredients (structured) | ✓ Available |
| NADAC pharmacy acquisition price (CMS) | — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey. |
| Orange Book / therapeutic-equivalence data | — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope. |
| HCPCS J-code billing crosswalk | — Not published for this NDC Most self-administered / retail products have no J-code — that is normal. |
| Medicaid utilization (CMS SDUD) | — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold. |