Home NDC 51393-5001-3 Allergy
Product NDC 51393-5001
Requested package NDC 51393-5001-3
11-digit product format 513935001
Labeler code 51393
Product ID 51393-5001_4b453b93-21bd-b234-e063-6294a90afd0b
Type HUMAN OTC DRUG
Nonproprietary name Urtica Dioica, Althaea Officinalis Root, Inula Helenium Root, Angelica Archangelica Root, Pine Needle Oil (Pinus Sylvestris), Sodium Chloride, and Silicon Dioxide
Dosage form SOLUTION/ DROPS
Route SUBLINGUAL
Labeler Forces of Nature
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-02-01
Substance URTICA DIOICA WHOLE; ALTHAEA OFFICINALIS ROOT; INULA HELENIUM ROOT; ANGELICA ARCHANGELICA ROOT; PINE NEEDLE OIL (PINUS SYLVESTRIS); SODIUM CHLORIDE; SILICON DIOXIDE
Active strength 8; 34; 55; 89; 89; 55; 89 [hp_C]/100mL; [hp_C]/100mL; [hp_C]/100mL; [hp_C]/100mL; [hp_C]/100mL; [hp_C]/100mL; [hp_C]/100mL
NDC exclude flag No
Listing certified through 2027-12-31
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 Allergy
Brand name suffix Maximum Strength
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength URTICA DIOICA WHOLE 8 [hp_C]/100mL ALTHAEA OFFICINALIS ROOT 34 [hp_C]/100mL INULA HELENIUM ROOT 55 [hp_C]/100mL ANGELICA ARCHANGELICA ROOT 89 [hp_C]/100mL PINE NEEDLE OIL (PINUS SYLVESTRIS) 89 [hp_C]/100mL SODIUM CHLORIDE 55 [hp_C]/100mL SILICON DIOXIDE 89 [hp_C]/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 7 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51393-5001-1 AllergyMaximum Strength 10 mL in 1 BOTTLE, DISPENSING SOLUTION/ DROPS 10 4 51393-5001-1 AllergyMaximum Strength 1 in 1 CARTON SOLUTION/ DROPS 1 4 51393-5001-3 AllergyMaximum Strength 30 mL in 1 BOTTLE, DISPENSING SOLUTION/ DROPS 30 4 51393-5001-3 AllergyMaximum Strength 1 in 1 CARTON SOLUTION/ DROPS 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51393-5001 ALLERGY MAXIMUM STRENGTH (URTICA DIOICA, ALTHAEA OFFICINALIS ROOT, INULA HELENIUM ROOT, ANGELICA ARCHANGELICA ROOT, PINE NEEDLE OIL (PINUS SYLVESTRIS), SODIUM CHLORIDE, AND SILICON DIOXIDE) SOLUTION/ DROPS [FORCES OF NATURE] 2 Current NDC, Legacy NDC, 4 package rows 20210929_122ca23e-43f1-4e5c-afc2-1418b1717679.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 Marketing start Marketing end Sample Exclude flag Status 51393-5001-3 51393500103 1 BOTTLE, DISPENSING in 1 CARTON (51393-5001-3) / 30 mL in 1 BOTTLE, DISPENSING 2021-10-15 0000-00-00 No No Current