Home NDC 43857-0036 Tri Estrogen
Product NDC 43857-0036
11-digit product format 438570036
Labeler code 43857
Product ID 43857-0036_728a4523-acd6-49d9-a153-7726ffe58ca4
Type HUMAN OTC DRUG
Nonproprietary name Folliculinum, Oophorinum,
Dosage form SPRAY
Route ORAL
Labeler BioActive Nutritional
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2012-06-01
Substance ESTRONE; SUS SCROFA OVARY
Active strength 6; 6 [hp_X]/mL; [hp_X]/mL
NDC exclude flag No
Listing certified through 2027-12-31
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 · 8 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 2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 43857-0036-1 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 43857-0036-1 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 43857-0036-1 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 43857-0036-1 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base Tri Estrogen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ESTRONE 6 [hp_X]/mL SUS SCROFA OVARY 6 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2DI9HA706A Internal UNII lookup S7YTV04R8O 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 43857-0036-1 Tri Estrogen 30 mL in 1 BOTTLE, SPRAY SPRAY 30 5
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ESTRONE ACTIVE INGREDIENT 2DI9HA706A TRI ESTROGEN (FOLLICULINUM, OOPHORINUM,) SPRAY [BIOACTIVE NUTRITIONAL] 1 SUS SCROFA OVARY ACTIVE INGREDIENT S7YTV04R8O TRI ESTROGEN (FOLLICULINUM, OOPHORINUM,) SPRAY [BIOACTIVE NUTRITIONAL] 1 ESTRONE ACTIVE MOIETY 2DI9HA706A TRI ESTROGEN (FOLLICULINUM, OOPHORINUM,) SPRAY [BIOACTIVE NUTRITIONAL] 1 SUS SCROFA OVARY ACTIVE MOIETY S7YTV04R8O TRI ESTROGEN (FOLLICULINUM, OOPHORINUM,) SPRAY [BIOACTIVE NUTRITIONAL] 1 CITRIC ACID MONOHYDRATE INACTIVE INGREDIENT 2968PHW8QP TRI ESTROGEN (FOLLICULINUM, OOPHORINUM,) SPRAY [BIOACTIVE NUTRITIONAL] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX TRI ESTROGEN (FOLLICULINUM, OOPHORINUM,) SPRAY [BIOACTIVE NUTRITIONAL] 1 SODIUM BENZOATE INACTIVE INGREDIENT OJ245FE5EU TRI ESTROGEN (FOLLICULINUM, OOPHORINUM,) SPRAY [BIOACTIVE NUTRITIONAL] 1 WATER INACTIVE INGREDIENT 059QF0KO0R TRI ESTROGEN (FOLLICULINUM, OOPHORINUM,) SPRAY [BIOACTIVE NUTRITIONAL] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43857-0036 TRI ESTROGEN (FOLLICULINUM, OOPHORINUM,) SPRAY [BIOACTIVE NUTRITIONAL] 4 Current NDC, Legacy NDC, 1 package rows 20240913_edf8db66-2bd3-46e8-9567-8883184bcdc3.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 Marketing end Sample Exclude flag Status 43857-0036-1 43857003601 30 mL in 1 BOTTLE, SPRAY (43857-0036-1) 30 ml 2016-09-13 0000-00-00 No No Current