Eye Makeup Remover

Product NDC
85161-300
11-digit product format
851610300
Labeler code
85161
Product ID
85161-300_4cea923c-ceea-f282-e063-6294a90a172c
Type
HUMAN OTC DRUG
Nonproprietary name
allantoin
Dosage form
LIQUID
Route
TOPICAL
Labeler
Longway Technology(Guangzhou) Co., Ltd
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-03-13
Substance
ALLANTOIN
Active strength
.05 g/100mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct85161-300DDiscontinued by firm2026-08-17
excluded packagepackage85161-30085161-300-04DDiscontinued by firm2026-08-17

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85161-300-04Eye Makeup Remover118 mL in 1 PACKAGELIQUID1181

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
85161-300-0485161030004118 mL in 1 PACKAGE118 mlHistorical