85248-208 update

Manufacturer
Jiangxi Yudexi Pharmaceutical Co., LTD | Jiangxi Zhongletang Pharmaceuticals Co.,Ltd.
Effective date
2026-05-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:57:19

Label at a glance#

ProductLixuhya MILIA REMOVER ESSENCE
Active ingredientSALICYLIC ACID
Label structure12 sections

Dosage and administration

L.Cleanse and dry the affected skin area thoroughly. 2.Apply a thin layer of the product directly onto the milia (skin bumps) once or twice daily, as needed. 3.Gently massage until fully absorbed. 4.For best results, use consistently for 4 weeks.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 1%

Purpose

OTC - PURPOSE SECTION

Milia Remover

Use

INDICATIONS & USAGE SECTION

For the removal of milia (skin bumps)
Aids in exfoliating dead skin cells
Helps smooth skin texture

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

Do not apply to broken, irritated,or sunburned skin.
Excessive drying or peeling may occur.
If severe irritation develops

When Using

OTC - WHEN USING SECTION

Avoid contact with eyes, lips, and mucous membranes.
If contact occurs,rinse thoroughly with water.
Do not apply to broken, irritated,or sunburned skin.
Excessive drying or peeling may occur.
If severe irritation develops,discontinue use.
Keep out of reach of children.

Stop Use

OTC - STOP USE SECTION

Condition worsens or does not improve within 4 weeks.
Severe redness, burning, or swelling occurs

Ask Doctor

OTC - ASK DOCTOR SECTION

ask a doctor if condition worsens or does not improve within 4 weeks.
Severe redness, burning, or swelling occurs.

If pregnant or breast-feeding, ask a health professional before use.

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

L.Cleanse and dry the affected skin area thoroughly.
2.Apply a thin layer of the product directly onto the milia (skin bumps) once or twice daily, as needed.
3.Gently massage until fully absorbed.
4.For best results, use consistently for 4 weeks.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Dextrin, Xanthan Gum,Amylopectin, Tocopheryl Acetate,Water.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047362salicylic acid 1 % Topical SolutionPSN2
1047362salicylic acid 10 MG/ML Topical SolutionSCD2
1047362salicylic acid 1 % Topical SolutionSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136979843981897GTIN-13: 6979843981897
EAN-13: 6979843981897
GTIN storage (14 digits): 06979843981897
5c790ca2685c5189959c9cd0e649caf8.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85248-208-01Lixuhya MILIA REMOVER ESSENCE40 mL in 1 BOTTLELIQUID402

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85248-20885248-208-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
Lixuhya MILIA REMOVER ESSENCESALICYLIC ACID 1% MILIA REMOVER ESSENCEJiangxi Yudexi Pharmaceutical Co., LTD51872c01-804c-a29f-e063-6294a90ae5462026-05-13WarningsExact identifier
ndc (package): 85248-208-01
ndc (product): 85248-208
ndc11 (package): 85248020801
spl id: 51bfd185-1937-c94b-e063-6394a90ac4c3
spl set id: 51872c01-804c-a29f-e063-6294a90ae546

Reported adverse events (FAERS/openFDA)#

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