Package 81923-366-00

Brand: powerect lidocaine male delay

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 81923-366-00
Digits Only 8192336600
Product NDC 81923-366
Product ID 81923-366_0976dfc5-c35a-11fe-e063-6294a90aa2bb
Description

15 mL in 1 BOTTLE, SPRAY (81923-366-00)

Marketing

Marketing Status
Marketed Since 2022-10-03
Brand powerect lidocaine male delay
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

POWERECT Lidocaine Male Delay ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "0976dfc5-c35a-11fe-e063-6294a90aa2bb", "openfda": {"upc": ["0847878002527"], "unii": ["V13007Z41A"], "spl_set_id": ["42e0c40f-1efd-45ef-815d-53d193d720eb"], "manufacturer_name": ["SKINS SEXUAL HEALTH LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 mL in 1 BOTTLE, SPRAY (81923-366-00)", "package_ndc": "81923-366-00", "marketing_start_date": "20221003"}], "brand_name": "POWERECT Lidocaine Male Delay", "product_id": "81923-366_0976dfc5-c35a-11fe-e063-6294a90aa2bb", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "81923-366", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "SKINS SEXUAL HEALTH LIMITED", "product_type": "HUMAN OTC DRUG", "brand_name_base": "POWERECT Lidocaine Male Delay", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221003", "listing_expiration_date": "20261231"}