Active Ingredients
Ketoconazole 1% Anti-dandruff shampoo
Lanimpress1%ketoconazoleantidandruffshampoo
FDA Label NDC 84372-039
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Zhumeng Times Technology Co., Ltd. for the product Lanimpress1%ketoconazoleantidandruffshampoo (NDC 84372-039). 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 active ingredients, purpose, uses, warnings, dosage and administration, do not use, when using section, stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
controls flaking, scaling and itching associated with dandruff
Uses
wet hair thoroughly
apply shampoo, generously lather,rinse thoroughiy. Repeat
use every 3-4 days for up to 8 weeks or as directed by a doctor. Then use oniy as needed to controt dandruff
Warnings
For external use only
Do not use
on scalp that is broken or inflamed
if you are allergic to ingredients in this product
Dosage And Administration
For external use only.
Do Not Use
Stop use and ask a doctor if rash occurs
When Using Section
rash appears
condition worsens or does not improve in 2-4 weeks.
Stop Use
Do not use
on scalp that is broken or inflamed
if you are allergic to ingredients in this product
Keep Out Of Reach Of Children
Keep out of reach of children.lf swallowed, get medical help or contacta Poison Control Center right away.
Inactive Ingredients
benzyl alcohol, BHT, blue 1, citric acid,cocamide MEA, fragrance, glycol distearate, hydrochloricacid, hydroxypropyl methylcellulose, polyquaternium-7, sodium chioride, sodium cocoyi sarcosinate, sodium hydroxide, sodiumlaureth sulfate, tetrasodium EDTA, waterCAPRYLATE,CARBOMER,METHYLPARABEN,TRIETHANOLAMINE,SODIUM HYALURONATE,DISODIUM EDTA，water
Principal Display Panel
84372-039-02 (84372 039 01)
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