Over-the-counter drug · OTC MONOGRAPH DRUG
Optimel Manuka Forte Eye Gel (glycerin) NDC 73024-429
Glycerin 2 mg/mL · Gel · Ophthalmic · Melcare Biomedical Pty Ltd
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 73024-429-10 | 73024042910 | 1 BOTTLE, DROPPER in 1 CARTON (73024-429-10) / 10 mL in 1 BOTTLE, DROPPERMarketed from Jul 19, 2019 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
- Optimel Manuka Forte Eye Gel
- Generic name (nonproprietary)
- glycerin
- Active ingredients
- Glycerin — 2 mg/mL
- Dosage form
- Gel
- Route
- Ophthalmic
- Labeler
- Melcare Biomedical Pty Ltd
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication M 014
- Marketing start
- Listing expires
- Other FDA classes
- Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Glycerol (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
- Identifiers
- Product ID 73024-429_4cc2d65c-f837-1869-e063-6294a90a108bSPL ID 4cc2d65c-f837-1869-e063-6294a90a108bSPL set ID 8e0ed6e8-51fc-7c5b-e053-2a95a90a35a9RxCUI 2179641UNII PDC6A3C0OX
- Pharmacologic class
- Non-Standardized Chemical Allergen
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. Ophthalmic products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N473024042910followed by a unit qualifier and the quantityPackage 73024-0429-10. 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 s for the temporary relief of burning and irritation due to dryness of the eye. for use as a protectant against further irritation or to relieve dryness of the eye.
Excerpt only. Read the full label for complete information.
Other NDCs under M 014
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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| ear dropscarbamide peroxide 6.5% | Carbamide peroxide .065 mg/mL | LiquidAuricular (Otic) | Bionpharma Inc. | 69452-377 |
| Family Wellness Earwax Removal Earwax and Bulbcarbamide peroxide | — | Kit | Family Dollar Services Inc | 55319-835 |
| Freskaro Earwax Removal Aidcarbamide peroxide 6.50% kit | Carbamide peroxide 6.5 g/100mL | LiquidAuricular (Otic) | Pharma Nobis, LLC | 82645-097 |
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| Clinere Ear Wax Removercarbamide peroxide | Carbamide peroxide .065 g/mL | LiquidAuricular (Otic) | Quest Products | 68229-102 |
| XIMONTH Wart Removerglycerin | Artemisia vulgaris root .004 mg/20mg + 2 more ingredients | OintmentTopical | Shantou Ximonth Biotechnology Co., Ltd. | 84989-004 |
| Earwax Removal Dropscarbamide peroxide 6.5% | Carbamide peroxide .065 mg/mL | LiquidAuricular (Otic) | Pharma Nobis, LLC | 82645-910 |
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