Home NDC 69710-165 SYMBIO PARA/ROQUEFORTI DROPS
Product NDC 69710-165
11-digit product format 697100165
Labeler code 69710
Product ID 69710-165_40e5e3bf-76fa-7552-e063-6294a90af768
Type HUMAN OTC DRUG
Nonproprietary name Candida parapsilosis, Penicillium roqueforti
Dosage form LIQUID
Route ORAL
Labeler Symbiopathic
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2023-10-08
Substance CANDIDA PARAPSILOSIS; PENICILLIUM ROQUEFORTI
Active strength 4; 4 [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 69710-165-11 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 69710-165-11 367a005e9d99…383a685ebd0f…
Additional Listing Data#
Finished product Yes
Brand name base SYMBIO PARA/ROQUEFORTI DROPS
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PENICILLIUM ROQUEFORTI 4 [hp_X]/mL CANDIDA PARAPSILOSIS 4 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 7ORP6R724L Internal UNII lookup 0KZ676D44N Internal UNII lookup
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 69710-165-11 SYMBIO PARA/ROQUEFORTI DROPS 10 mL in 1 BOTTLE LIQUID 10 3 69710-165-11 SYMBIO PARA/ROQUEFORTI DROPS 1 in 1 CARTON LIQUID 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69710-165 SYMBIO PARA/ROQUEFORTI DROPS (CANDIDA PARAPSILOSIS, PENICILLIUM ROQUEFORTI) LIQUID [SYMBIOPATHIC] 2 Current NDC, 2 package rows 20241213_0788c3b6-d876-b337-e063-6294a90acd3a.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 69710-165-11 69710016511 1 BOTTLE in 1 CARTON (69710-165-11) / 10 mL in 1 BOTTLE 1 bottle 2023-10-08 No No Current