LANIMPRESS1%KETOCONAZOLEANTIDANDRUFFSHAMPOO lotion

lanimpress1%ketoconazoleantidandruffshampoo by

Drug Labeling and Warnings

lanimpress1%ketoconazoleantidandruffshampoo by is a Otc medication manufactured, distributed, or labeled by Shenzhen Zhumeng Times Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Ketoconazole 1% Anti-dandruff shampoo

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

INGREDIENTS AND APPEARANCE

LANIMPRESS1%KETOCONAZOLEANTIDANDRUFFSHAMPOO 
lanimpress1%ketoconazoleantidandruffshampoo lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84372-039
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
KETOCONAZOLE (UNII: R9400W927I) (KETOCONAZOLE - UNII:R9400W927I)	KETOCONAZOLE	5 g  in 125 mL

Inactive Ingredients
Ingredient Name	Strength
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
TROLAMINE (UNII: 9O3K93S3TK)
EDETATE SODIUM (UNII: MP1J8420LU)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
SODIUM COCOYL SARCOSINATE (UNII: 1R9DUY89CZ)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
WATER (UNII: 059QF0KO0R)
IVERMECTIN (UNII: 8883YP2R6D)
METHYLPARABEN (UNII: A2I8C7HI9T)
8-PENTADECANONE (UNII: QO7H8D8OSB)
HYDROCHLORIC ACID (UNII: QTT17582CB)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
HYPROMELLOSES (UNII: 3NXW29V3WO)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ACONITIC ACID (UNII: 93371T1BXP)
FRAGRANCE 13576 (UNII: 5EM498GW35)
BENZYL ALCOHOL (UNII: LKG8494WBH)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84372-039-01	125 mL in 1 BOX; Type 0: Not a Combination Product	09/02/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	09/02/2024

Labeler - Shenzhen Zhumeng Times Technology Co., Ltd. (631852731)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Zhumeng Times Technology Co., Ltd.		631852731	manufacture(84372-039)