87983-002 NDC - SKIN SMOOTHING CARE (CENTELLA ASIATICA TRITERPENOIDS)

Drug Information

  • Product NDC: 87983-002
  • Proprietary Name: Skin Smoothing Care
  • Non Proprietary Name: CENTELLA ASIATICA TRITERPENOIDS
  • Active Ingredient(s): 2 g/100g BETAINE; .2 g/100g HYALURONIC ACID; 5 g/100g TREFOIL FACTOR 1; .3 g/100g ALLANTOIN; .25 g/100g ARGININE; 8 g/100g CENTELLA ASIATICA TRITERPENOIDS; 3 g/100g CERAMIDE NP; 3 g/100g PEPTIDE-T; .5 g/100g TOCOPHEROL; 1 g/100g ASIATICOSIDE; 2 g/100g REHMANNIA GLUTINOSA ROOT
  • Administration Route(s): TOPICAL
  • Dosage Form(s): CREAM
  • Pharmacy Class(es): Methylating Activity [MoA]; Methylating Agent [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Haikou Flash Purchase Star Cross-Border Trade Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: 505G(a)(3)
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:9/2/2026

Package Information

No. Package Code Package Description Billing Unit
187983-002-0150 g in 1 BOTTLE (87983-002-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC87983-002The 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 NAMEHUMAN OTC DRUGIndicates 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 NAMESkin Smoothing CareThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECENTELLA ASIATICA TRITERPENOIDSThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECREAMThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE9/2/2026This 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 NAMEHaikou Flash Purchase Star Cross-Border Trade Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEBETAINE; HYALURONIC ACID; TREFOIL FACTOR 1; ALLANTOIN; ARGININE; CENTELLA ASIATICA TRITERPENOIDS; CERAMIDE NP; PEPTIDE-T; TOCOPHEROL; ASIATICOSIDE; REHMANNIA GLUTINOSA ROOTAn 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 STRENGTH2; .2; 5; .3; .25; 8; 3; 3; .5; 1; 2 
ACTIVE INGRED UNITg/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g 
PHARM CLASSESMethylating Activity [MoA], Methylating Agent [EPC] 

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This page was last updated on: 9/11/2026

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