MEOLY Milia Remover 30 ml

Product NDC: 83818-007
11-digit product format: 838180007
Labeler code: 83818
Product ID: 83818-007_27b78b20-5c66-10ad-e063-6394a90ad22e
Type: HUMAN OTC DRUG
Nonproprietary name: Milia Remover
Dosage form: LIQUID
Route: TOPICAL
Labeler: Shenzhen Xinxin Yunhai Technology Co., Ltd.
Application: M028
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2024-11-25
Substance: DIDECYLDIMONIUM CHLORIDE
Active strength: .025 g/100mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: MEOLY Milia Remover 30 ml
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
DIDECYLDIMONIUM CHLORIDE	.025 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
JXN40O9Y9B	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
27b78b20-5c65-10ad-e063-6394a90ad22e	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
83818-007-01	MEOLY Milia Remover 30 ml	30 mL in 1 BOTTLE	LIQUID	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
83818-007	MEOLY MILIA REMOVER 30 ML (MILIA REMOVER) LIQUID [SHENZHEN XINXIN YUNHAI TECHNOLOGY CO., LTD.]	1	Current NDC, 1 package rows	20241127_27b78b20-5c65-10ad-e063-6394a90ad22e.zip

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 16 of 16 · 305 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ulensy Corn Callus and Wart Remover	CORN CALLUS AND WART REMOVER	Shenzhen Xinxin Yunhai Technology Co., Ltd.	0f3353ef-e105-7bd4-e063-6394a90a2562	2024-01-18	Warnings	Exact identifier application number: M028
WARTRIN Wart Remover	SALICYLIC ACID	BALBOA COMPANIES LLC	62c99f48-3dc1-4b41-8bc4-e93e2decadd9	2023-11-11	Warnings	Exact identifier application number: M028
UFORIC Wart Remover	SALICYLIC ACID	UFORIC HEALTH LLC	0d06cac6-5296-4d8a-b59e-966baac6be5f	2023-11-06	Warnings	Exact identifier application number: M028
WARTOVIR Wart Remover	SALICYLIC ACID	BALBOA COMPANIES LLC	2dbf5b40-d759-4c37-8dfe-3b65a7e6dbb6	2023-11-06	Warnings	Exact identifier application number: M028
VerruStat Wart Remover	SALICYLIC ACID	Clinical Therapeutic Solutions	16607d6e-6a5f-4b03-b38c-3610aef9b165	2023-11-05	Warnings	Exact identifier application number: M028

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
JXN40O9Y9B	DIDECYLDIMONIUM CHLORIDE	7173-51-5	DIDECYLDIMONIUM CHLORIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
83818-007-01	83818000701	30 mL in 1 BOTTLE (83818-007-01)	30 ml	2024-11-25	No	No	Current