Home NDC 43857-0364 Bio Holly
Product NDC 43857-0364
11-digit product format 438570364
Labeler code 43857
Product ID 43857-0364_8d6da373-b14a-4a25-ba17-f5b479017da8
Type HUMAN OTC DRUG
Nonproprietary name Ilex Aquifolium (Holly), Flos
Dosage form LIQUID
Route ORAL
Labeler BioActive Nutritional, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-04-01
Marketing end 0000-00-00
Substance ILEX AQUIFOLIUM FRUITING TOP
Active strength 6 [hp_X]/mL
NDC exclude flag No
Listing certified through 2020-12-31
Current FDA listing Historical FDA.report record 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 · 10 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 43857-0364-1 D Discontinued by firm d630ba8d3edf…732f749b63fb…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 43857-0364-1 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 43857-0364-1 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 43857-0364-1 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 43857-0364-1 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ILEX AQUIFOLIUM FRUITING TOP ACTIVE INGREDIENT 147AL91LPR BIO HOLLY (ILEX AQUIFOLIUM (HOLLY), FLOS) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 2 ILEX AQUIFOLIUM FRUITING TOP ACTIVE MOIETY 147AL91LPR BIO HOLLY (ILEX AQUIFOLIUM (HOLLY), FLOS) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 2 ALCOHOL INACTIVE INGREDIENT 3K9958V90M BIO HOLLY (ILEX AQUIFOLIUM (HOLLY), FLOS) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 2 WATER INACTIVE INGREDIENT 059QF0KO0R BIO HOLLY (ILEX AQUIFOLIUM (HOLLY), FLOS) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43857-0364 BIO HOLLY (ILEX AQUIFOLIUM (HOLLY), FLOS) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 4 Legacy NDC 20230608_7eda4853-640b-4190-a6f5-ee9b068ed429.zip