Home NDC 69710-215 SYMBIO FIRM DROPS
Product NDC 69710-215
11-digit product format 697100215
Labeler code 69710
Product ID 69710-215_40e5ceff-3909-a297-e063-6394a90af124
Type HUMAN OTC DRUG
Nonproprietary name Bacillus firmus
Dosage form LIQUID
Route ORAL
Labeler Symbiopathic
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2016-08-25
Substance BACILLUS FIRMUS
Active strength 6 [hp_X]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base SYMBIO FIRM DROPS
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BACILLUS FIRMUS 6 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination D6U864H4DT 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 69710-215-11 SYMBIO FIRM DROPS 1 in 1 CARTON LIQUID 1 4 69710-215-11 SYMBIO FIRM DROPS 5 mL in 1 BOTTLE LIQUID 5 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69710-215 SYMBIO FIRM DROPS (BACILLUS FIRMUS) LIQUID [SYMBIOPATHIC] 3 Current NDC, 2 package rows 20241213_29047c78-2030-8614-e063-6394a90a9c85.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 69710-215-11 69710021511 1 BOTTLE in 1 CARTON (69710-215-11) / 5 mL in 1 BOTTLE 1 bottle 2016-08-25 No No Current