FDA.reportPublic FDA data

LANIMPRESS Dark spot correctorcream

Manufacturer
Shenzhen Zhumeng Times Technology Co., Ltd.
Effective date
2024-09-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:19:37

Label at a glance#

ProductPrivate backya-rd relaxation gel
Active ingredientLAURYL ALCOHOL
Label structure12 sections

Indications and uses

Apply around the anus and wait 5 minutes

Dosage and administration

For external use only.

Label contents#

Full prescribing information#

Active ingredients

COMPONENTS

lauryl alcohol polye-ther-9 5%

Purpose

OTC - PURPOSE SECTION

Loose anal muscles

Uses

INDICATIONS & USAGE SECTION

Apply around the anus and wait 5 minutes

Contraindications, Precautions, Warnings, and Instructions

WARNINGS SECTION

Prohibit ingestion by mouth.

Do not put into eyes or ears.

No contact with wounds.

Dosage and administration

DOSAGE & ADMINISTRATION SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

Skin irritation occurs, wash with water, discontinue use

If symptoms do not improve, seek medical attention immediately

When using section

OTC - WHEN USING SECTION

Skin irritation occurs, wash with water, discontinue use

If symptoms do not improve, seek medical attention immediately。

Allow 5 minutes for the product to take effect

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,PEG-7 coco-nut glycerin,PEG-4o hydrogenated pi-edmont oil,ethylene glycol phenyl ether,aminomethylpropanol,propionic acid/C10-30,alkyl acr-ylic polymer,carbomer,ethyl he-xyl glycerol,oat kernel extract,menthol oil,glycerin,hop oil,di-pentene

stop use

OTC - STOP USE SECTION

Wound breaks

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If sxralowed, get medical help or contact a Poison Conirol Cenler ngiht away.

RECENT MAJOR CHANGES SECTION

Package

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
d723478e-ad4a-ec23-6bd7-cfe33e1e3840Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84372-057-012025-07-29C16284748780-13b156c62-2fd0-fb37-e063-e6dba90a4e07209744ee-263b-6fcc-e063-6394a90af9ca

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84372-057-01Private backya-rd relaxation gel30 mg in 1 BOXGEL303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84372-057PRIVATE BACKYA-RD RELAXATION GEL GEL [SHENZHEN ZHUMENG TIMES TECHNOLOGY CO., LTD.]31 package rows20240918_209744ee-263b-6fcc-e063-6394a90af9ca.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84372-05784372-057-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYETHYLENE GLYCOL 3350G2M7P15E5PIACT
WATER059QF0KO0RIACT
ALKYLSEVINJKS3UE1KPGIACT
MENTHOL, (+)-C6B1OE8P3WIACT
PROPIONIC ACIDJHU490RVYRIACT
HOPS OIL06JI9W529SIACT
N-ETHYLHEXEDRONETAX3KSX6GYIACT
OATZ6J799EAJKIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
HYDROGENATED RAPESEED OILK168T6Y0YUIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
2-PENTENEY5RK21VDPEIACT
LAURYL ALCOHOL178A96NLP2ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2223571c-17da-a93c-e063-6394a90aeb22209744ee-263b-6fcc-e063-6394a90af9ca2024-09-15WarningsExact identifier
spl id: 2223571c-17da-a93c-e063-6394a90aeb22
spl set id: 209744ee-263b-6fcc-e063-6394a90af9ca

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.