Home NDC 85869-123 Plaque identifying
Product NDC 85869-123
11-digit product format 858690123
Labeler code 85869
Product ID 85869-123_37eeb656-22f2-7372-e063-6394a90ad041
Type HUMAN OTC DRUG
Nonproprietary name Plaque identifying
Dosage form POWDER, DENTIFRICE
Route DENTAL
Labeler Shenzhen Yagao Technology Co., Ltd.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-06-24
Substance SORBITOL; WATER
Active strength 1; 1 g/g; g/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Plaque identifying
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength WATER 1 g/g SORBITOL 1 g/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 059QF0KO0R Internal UNII lookup 506T60A25R Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85869-123-47 Plaque identifying 5 in 1 CARTON POWDER, DENTIFRICE 5 1 85869-123-47 Plaque identifying 1 g in 1 BOX, UNIT-DOSE POWDER, DENTIFRICE 1 1
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 85869-123-47 85869012347 5 BOX, UNIT-DOSE in 1 CARTON (85869-123-47) / 1 g in 1 BOX, UNIT-DOSE 2025-07-03 No No Current