83566-402 NDC - LEXI WHITE BEAUTY 5% MINOXIDIL SERUM ()

Drug Information

  • Product NDC: 83566-402
  • Proprietary Name: Lexi White Beauty 5% Minoxidil Serum
  • Non Proprietary Name:
  • Active Ingredient(s): .05 g/mL MINOXIDIL
  • Administration Route(s):
  • Dosage Form(s):
  • Pharmacy Class(es): Arteriolar Vasodilation [PE]; Arteriolar Vasodilator [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Guangdong Aimu Biological Technology Co., Ltd
Product Type:
FDA Application Number: ANDA209074
Marketing Category: ANDA
Start Marketing Date:1/8/2024
End Marketing Date:1/9/2024

Package Information

No. Package Code Package Description Billing Unit
183566-402-011 CANISTER in 1 BOX (83566-402-01) / 30 mL in 1 CANISTER
283566-402-0130 mL in 1 BOTTLE (83566-402-01)
383566-402-021 CANISTER in 1 BOX (83566-402-02) / 50 mL in 1 CANISTER
483566-402-0260 mL in 1 BOTTLE (83566-402-02)
583566-402-031 CANISTER in 1 BOX (83566-402-03) / 60 mL in 1 CANISTER
683566-402-0380 mL in 1 BOTTLE (83566-402-03)
783566-402-041 CANISTER in 1 BOX (83566-402-04) / 80 mL in 1 CANISTER
883566-402-04100 mL in 1 BOTTLE (83566-402-04)
983566-402-051 CANISTER in 1 BOX (83566-402-05) / 100 mL in 1 CANISTER
1083566-402-05120 mL in 1 BOTTLE (83566-402-05)
1183566-402-061 CANISTER in 1 BOX (83566-402-06) / 120 mL in 1 CANISTER
1283566-402-06150 mL in 1 BOTTLE (83566-402-06)
1383566-402-071 CANISTER in 1 BOX (83566-402-07) / 150 mL in 1 CANISTER
1483566-402-07180 mL in 1 BOTTLE (83566-402-07)
1583566-402-081 CANISTER in 1 BOX (83566-402-08) / 180 mL in 1 CANISTER
1683566-402-08200 mL in 1 BOTTLE (83566-402-08)
1783566-402-091 CANISTER in 1 BOX (83566-402-09) / 200 mL in 1 CANISTER
1883566-402-09220 mL in 1 BOTTLE (83566-402-09)
1983566-402-101 CANISTER in 1 BOX (83566-402-10) / 220 mL in 1 CANISTER

NDC Record

Field Name Field Value Definition
PRODUCT NDC83566-402The 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 NAMELexi White Beauty 5% Minoxidil SerumThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/8/2024This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEANDAProduct 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 NUMBERANDA209074This 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 NAMEGuangdong Aimu Biological Technology Co., LtdName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC83566-402The 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 NAMELexi White Beauty Hair Regrowth 5% Minoxidil FoamThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/23/2024This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct 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 NUMBER505G(a)(3)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 NAMEGuangdong Aimu Biological Technology Co., LtdName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 5/26/2025

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