Otc - Purpose
Relieve Itching
Drmitsui Vaginal Probiotics Gel
FDA Label NDC 85031-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Zhuoyue Trading Co., Ltd for the product Drmitsui Vaginal Probiotics (NDC 85031-010). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - purpose, otc - keep out of reach of children, otc - active ingredient, warnings, indications & usage, inactive ingredient, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Keep Out Of Reach Of Children
keep out of reach of children
Otc - Active Ingredient
Rosa Rugosa Flower Water
Centella Asiatica Extract
Purslane (Portulaca Oleracea) Extract
Warnings
WARNINGSFor external use only. Discontinue useimmediately if an allergic reaction occurs
Indications & Usage
Clean the perineal area before use. Assumea squatting or lying position, relax yourbody, gently insert the applicator into thevagina, and gently dispense the gel
Inactive Ingredient
INACTIVE INGREDIENTSWater, Longan (Euphoria Longana) FruitExtract, Glucose, Propylene Glycol, IsomaltOligosaccharide, Fructooligosaccharide,Inulin, Sodium Hyaluronate, HydrolysedSodium Hyaluronate, Hyaluronic Acid,Hydrolysed Hyaluronic Acid, AcetylatedSodium Hyaluronate, Cross-linked SodiumHyaluronate Polymer, Pro-vitamin B5,Rosa Rugosa Flower Water, CentellaAsiatica Extract, Purslane (PortulacaOleracea) Extract, Silver Lons, Carbomer,Triethanolamine.
Dosage & Administration
Useone applicator per night for a 7-daytreatment cycle.
Package Label.Principal Display Panel
Labeling (85031 010 01)
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