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  5. NDC Package Code: 77632-162-11 Bvibe

NDC Package 77632-162-11 Bvibe

Lidocaine Hcl Delay Spray Liquid Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
77632-162-11
Package Description:
59 mL in 1 BOTTLE, SPRAY
Product Code:
77632-162
Proprietary Name:
Bvibe
Non-Proprietary Name:
Lidocaine Hcl Delay Spray
Substance Name:
Lidocaine Hydrochloride
Usage Information:
Adults: Apply 3-10 sprays to penis head/shaft (focus on frenulum/tip) 10 minutes before intercourse. Start with 3 sprays to assess sensitivity. Shake bottle, spray directly or massage on. Allow 10 minutes absorption; wipe excess before oral sex. Wash off post-intercourse. Store at 68°-77°F, away from heat/sunlight.
11-Digit NDC Billing Format:
77632016211
Product Type:
Human Otc Drug
Labeler Name:
Private Label Productions Llc
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s):
LIDOCAINE HYDROCHLORIDE 9.94 mg/.1mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M017
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
07-15-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

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.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 77632-162-11?

The NDC Packaged Code 77632-162-11 is assigned to a package of 59 ml in 1 bottle, spray of Bvibe, a human over the counter drug labeled by Private Label Productions Llc. The product's dosage form is liquid and is administered via topical form.

Is NDC 77632-162 included in the NDC Directory?

Yes, Bvibe with product code 77632-162 is active and included in the NDC Directory. The product was first marketed by Private Label Productions Llc on July 15, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 77632-162-11?

The 11-digit format is 77632016211. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-277632-162-115-4-277632-0162-11