FDA label 82c2d9cd-e7ab-4603-959e-c3435b479210

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID
0ab551a2-f744-4278-92b4-97c5cb6fa504
SPL ID
82c2d9cd-e7ab-4603-959e-c3435b479210
Version
1
Effective date
2011-04-06
Source export date
2026-08-01
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/286b06ef66f7efdb8cdf48688678b429950d1b94558fe44fcd6cc6eb20c2100b/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:05:25

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

■ Bioisoflavone ① Only use for postmenopausal women ② Do not take in case of pregnancy or lactation ③Keep out of reach of children ④ Do not take if allergic to soy ⑤ Persons with estrogen-dependent cancers should not take product ■ N- acetylglucosamine : Do not take if allergic to crab