54860-525 NDC - SMART CARE LUXURY HAND SANITIZER CASHMERE CHAR (ALCOHOL)

Drug Information

Product NDC: 54860-525
Proprietary Name: Smart Care Luxury Hand Sanitizer Cashmere Char
Non Proprietary Name: alcohol
Active Ingredient(s): 70 mL/100mL ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY

Labeler Information

Field Name	Field Value
Labeler Name:	Shenzhen Lantern Scicence Co.,Ltd.
Product Type:	HUMAN OTC DRUG
FDA Application Number:	M003
Marketing Category:	OTC MONOGRAPH DRUG
Start Marketing Date:	10/19/2025

Package Information

No.	Package Code	Package Description	Billing Unit
1	54860-525-01	50 mL in 1 BOTTLE, SPRAY (54860-525-01)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	54860-525	This is the date that the labeler indicates was the start of its marketing of the drug product.
PRODUCT TYPE NAME	HUMAN OTC DRUG	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.
PROPRIETARY NAME	Smart Care Luxury Hand Sanitizer Cashmere Char	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.
NON PROPRIETARY NAME	alcohol	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.
DOSAGE FORM NAME	SPRAY	Name of Company corresponding to the labeler code segment of the Product NDC.
ROUTE NAME	TOPICAL	The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE	10/19/2025	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
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	M003	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	Shenzhen Lantern Scicence Co.,Ltd.	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	ALCOHOL	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.
ACTIVE NUMERATOR STRENGTH	70	Name of Company corresponding to the labeler code segment of the Product NDC.
ACTIVE INGRED UNIT	mL/100mL

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

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