83887-008 NDC - PRESSY TATTOO NUMBING CREAM ()

Drug Information

Product NDC: 83887-008
Proprietary Name: Pressy Tattoo Numbing Cream
Non Proprietary Name:
Active Ingredient(s): 5 g/100g LIDOCAINE
Administration Route(s):
Dosage Form(s):
Pharmacy Class(es): Amide Local Anesthetic [EPC]; Amides [CS]; Antiarrhythmic [EPC]; Local Anesthesia [PE]

Labeler Information

Field Name	Field Value
Labeler Name:	Changsha Beiliang E-commerce Co., Ltd
Product Type:
FDA Application Number:	M017
Marketing Category:	OTC MONOGRAPH DRUG
Start Marketing Date:	6/12/2025
End Marketing Date:	6/14/2025

Package Information

No.	Package Code	Package Description	Billing Unit
1	83887-008-01	60 g in 1 BOTTLE (83887-008-01)
2	83887-008-01	60 g in 1 BOTTLE (83887-008-01)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	83887-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	Pressy Tattoo Numbing Cream	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	6/12/2025	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	OTC MONOGRAPH DRUG	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBER	M017	This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAME	Changsha Beiliang E-commerce Co., Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC	83887-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	Pressy Tattoo Numbing Cream	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	6/12/2025	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	OTC MONOGRAPH DRUG	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBER	M017	This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAME	Changsha Beiliang E-commerce Co., Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 7/4/2025

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