Home NDC 55926-0027 emuaidMAX Concentrate
Product NDC 55926-0027
11-digit product format 559260027
Labeler code 55926
Product ID 55926-0027_9d31bf43-415d-410a-8c41-a641b9698849
Type HUMAN OTC DRUG
Nonproprietary name Silver
Dosage form LIQUID
Route TOPICAL
Labeler Speer Laboratories, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2023-03-01
Substance SILVER
Active strength 10 [hp_X]/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base emuaidMAX Concentrate
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SILVER 10 [hp_X]/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3M4G523W1G Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 55926-0027-2 emuaidMAX Concentrate 30 mL in 1 BOTTLE, PLASTIC LIQUID 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55926-0027 EMUAIDMAX CONCENTRATE (SILVER) LIQUID [SPEER LABORATORIES, LLC] 1 Current NDC, 1 package rows 20231114_1fe32c32-1694-4df6-aacc-3a70f4383b95.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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 55926-0027-2 55926002702 30 mL in 1 BOTTLE, PLASTIC (55926-0027-2) 30 ml 2023-03-01 No No Current