85031-010 NDC - DRMITSUI VAGINAL PROBIOTICS (VAGINAL PROBIOTICS)

Drug Information

Product NDC: 85031-010
Proprietary Name: DRMITSUI VAGINAL PROBIOTICS
Non Proprietary Name: VAGINAL PROBIOTICS
Active Ingredient(s): 3 g/100g CENTELLA ASIATICA ROOT; 3 g/100g PORTULACA OLERACEA SEED; 5 g/100g ROSA RUGOSA FLOWER BUD
Administration Route(s): TOPICAL
Dosage Form(s): GEL

Labeler Information

Field Name	Field Value
Labeler Name:	Guangzhou Zhuoyue Trading Co., Ltd
Product Type:	HUMAN OTC DRUG
FDA Application Number:	505G(a)(3)
Marketing Category:	OTC MONOGRAPH DRUG
Start Marketing Date:	4/12/2026

Package Information

No.	Package Code	Package Description	Billing Unit
1	85031-010-01	7 PATCH in 1 BOX (85031-010-01) / 3 g in 1 PATCH

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	85031-010	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	DRMITSUI VAGINAL PROBIOTICS	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAME	VAGINAL PROBIOTICS	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	GEL	The translation of the dosage form Code submitted by the firm.
ROUTE NAME	TOPICAL	The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE	4/12/2026	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	505G(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 NAME	Guangzhou Zhuoyue Trading Co., Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	CENTELLA ASIATICA ROOT; PORTULACA OLERACEA SEED; ROSA RUGOSA FLOWER BUD	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	3; 3; 5
ACTIVE INGRED UNIT	g/100g; g/100g; g/100g

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This page was last updated on: 6/19/2026

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