Vicks Zzzquil Kit
NDC Package 84126-306-03
Package Information
Vicks Zzzquil (diphenhydramine hydrochloride) kits is • take only one dose (30 mL) per day (24 hours) • only use dose cup provided adults & children 12 yrs & over30 mL at bedtime if needed or as directed by a doctorchildren under 12 yrsdo not use. This formulation utilizes a kit delivery system. Marketed by The Procter & Gamble Manufacturing Company, this product is identified by NDC 84126-306 and is authorized under FDA application M010.
Identification & Billing
- RxCUI: 1248354 - diphenhydrAMINE HCl 50 MG in 30 mL Oral Solution
- RxCUI: 1248354 - diphenhydramine hydrochloride 1.67 MG/ML Oral Solution
- RxCUI: 1248354 - diphenhydramine HCl 1.667 MG/ML Oral Solution
- RxCUI: 1248354 - diphenhydramine HCl 50 MG per 30 ML Oral Solution
- RxCUI: 1248356 - ZzzQuil NIGHTTIME SLEEP-AID 50 MG in 30 mL Oral Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 84126 - The Procter & Gamble Manufacturing Company
- 84126-306 - Vicks Zzzquil
- 84126-306-03 - 1 KIT in 1 CARTON * 2 BOTTLE, PLASTIC in 1 PACKAGE, COMBINATION (37000-500-24) / 354 mL in 1 BOTTLE, PLASTIC (37000-500-12)
- 84126-306 - Vicks Zzzquil
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 84126-306-03 identifies a specific commercial package of 1 kit in 1 carton * 2 bottle, plastic in 1 package, combination (37000-500-24) / 354 ml in 1 bottle, plastic (37000-500-12) of Vicks Zzzquil Nighttime Sleep-aid, a human over the counter drug labeled by The Procter & Gamble Manufacturing Company. This kit is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by The Procter & Gamble Manufacturing Company on July 15, 2024.
How is this The Procter & Gamble Manufacturing Company product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 84126030603. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.