Over-the-counter drug · OTC MONOGRAPH DRUG
Rite Aid Povidone Iodine (povidone iodine 10%) NDC 11822-3775
Povidone-iodine 100 mg/mL · Liquid · Topical · Rite Aid Corporation
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 11822-3775-7 | 11822377507 | 237 mL in 1 BOTTLE, PLASTIC (11822-3775-7)Marketed from Nov 14, 2017 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Rite Aid Povidone Iodine
- Generic name (nonproprietary)
- povidone iodine 10%
- Active ingredients
- Povidone-iodine — 100 mg/mL
- Dosage form
- Liquid
- Route
- Topical
- Labeler
- Rite Aid Corporation
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication M 003
- Marketing start
- Listing expires
- Identifiers
- Product ID 11822-3775_0c93bbb5-cb31-1f6e-e063-6394a90a39f5SPL ID 0c93bbb5-cb31-1f6e-e063-6394a90a39f5SPL set ID 5df6ff37-a4ea-d666-e053-2991aa0a9786RxCUI 312564UNII 85H0HZU99MUPC 0011822377577
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N411822377507followed by a unit qualifier and the quantityPackage 11822-3775-07. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Use First aid antiseptic to prevent infection in minor cuts and burns.
Excerpt only. Read the full label for complete information.
Other NDCs under M 003
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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