82385-104 NDC - AN12 SKIN THERAPY VITA-B ALOE SOOTHING GEL (GLYCERIN)

Drug Information

Product NDC: 82385-104
Proprietary Name: AN12 Skin Therapy Vita-B Aloe Soothing Gel
Non Proprietary Name: Glycerin
Active Ingredient(s): 2 g/100mL GLYCERIN
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Glycerol [CS]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Chemical Allergen [EPC]

Labeler Information

Field Name	Field Value
Labeler Name:	BESTVALUE Co., Ltd
Product Type:	HUMAN OTC DRUG
FDA Application Number:
Marketing Category:	UNAPPROVED DRUG OTHER
Start Marketing Date:	12/6/2021

Package Information

No.	Package Code	Package Description	Billing Unit
1	82385-104-01	300 mL in 1 BOTTLE, PUMP (82385-104-01)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	82385-104	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.
PRODUCT TYPE NAME	HUMAN OTC DRUG	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAME	AN12 Skin Therapy Vita-B Aloe Soothing Gel	This is the date that the labeler indicates was the start of its marketing of the drug product.
NON PROPRIETARY NAME	Glycerin	This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
DOSAGE FORM NAME	GEL	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.
ROUTE NAME	TOPICAL	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.
START MARKETING DATE	12/6/2021	Name of Company corresponding to the labeler code segment of the Product NDC.
MARKETING CATEGORY NAME	UNAPPROVED DRUG OTHER	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.
LABELER NAME	BESTVALUE Co., Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	GLYCERIN	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	2
ACTIVE INGRED UNIT	g/100mL
PHARM CLASSES	Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC]

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

This page was last updated on: 11/21/2025

Previous Code

Next Code