Over-the-counter drug · OTC MONOGRAPH DRUG
Certain Dri Clinical Strength Prescription Protection Rollon NDC 69693-734
Aluminum chloride 15 g/100mL · Liquid · Topical · Clarion Brands LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 69693-734-12 | 6969307341269693073412 | 1 CYLINDER in 1 CARTON (69693-734-12) / 35 mL in 1 CYLINDERMarketed from Dec 24, 2025 |
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)
- Certain Dri Clinical Strength Prescription Protection Rollon
- Generic name (nonproprietary)
- certain dri clinical strength prescription protection rollon
- Active ingredients
- Aluminum chloride — 15 g/100mL
- Dosage form
- Liquid
- Route
- Topical
- Labeler
- Clarion Brands LLCNDC labeler code 69693
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication M 017
- Marketing start
- Listing expires
- Identifiers
- Product ID 69693-734_46a1f92e-4412-3989-e063-6394a90a7038SPL ID 46a1f92e-4412-3989-e063-6394a90a7038SPL set ID 46a1f92e-4411-3989-e063-6394a90a7038UNII 3CYT62D3GA
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
N469693073412followed by a unit qualifier and the quantityPackage 69693-0734-12. 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)
extra effective at reducing underarm perspiration
Excerpt only. Read the full label for complete information.
About NDC 69693-734
- What is NDC 69693-734?
- 69693-734 is the product NDC for Certain Dri Clinical Strength Prescription Protection Rollon, Aluminum chloride 15 g/100mL liquid, listed with the FDA by Clarion Brands LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Certain Dri Clinical Strength Prescription Protection Rollon.
- What is the active ingredient?
- Aluminum chloride.
- Who is the labeler?
- Clarion Brands LLC, NDC labeler code 69693. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Certain Dri Clinical Strength Prescription Protection Rollon?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Other NDCs under M 017
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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