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NDC 67618-0183-06 Maximum Strength Betadine Clear .13; 1 mg/mL; mg/mL Details
Maximum Strength Betadine Clear .13; 1 mg/mL; mg/mL
Maximum Strength Betadine Clear is a TOPICAL SPRAY in the HUMAN OTC DRUG category. It is labeled and distributed by Atlantis Consumer Healthcare, Inc.. The primary component is BENZALKONIUM CHLORIDE; PRAMOXINE HYDROCHLORIDE.
Product Information
| NDC | 67618-0183 |
|---|---|
| Product ID | 67618-183_31b94a76-1536-47c0-ab03-e487c2625c58 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Maximum Strength Betadine Clear |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Benzalkonium Cl and Pramoxine HCl |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | SPRAY |
| Route | TOPICAL |
| Active Ingredient Strength | .13; 1 |
| Active Ingredient Units | mg/mL; mg/mL |
| Substance Name | BENZALKONIUM CHLORIDE; PRAMOXINE HYDROCHLORIDE |
| Labeler Name | Atlantis Consumer Healthcare, Inc. |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M003 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 67618-0183-06 (67618018306)
| NDC Package Code | 67618-183-06 |
|---|---|
| Billing NDC | 67618018306 |
| Package | 177 mL in 1 BOTTLE (67618-183-06) |
| Marketing Start Date | 2023-12-22 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |