ABC Balance Cure

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)

Brand name: ABC Balance Cure
Generic name: QUERCUS ACUTISSIMA SAP
Manufacturer: ABCPharm co.,LTD
Product type: HUMAN OTC DRUG
SPL set ID: 49d159e9-b532-7b8b-e063-6394a90a3712
SPL ID: 49e26874-0058-7724-e063-6294a90a0fa8
Version: 2
Effective date: 2026-02-02
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:25:51

Harmonized routes table
Harmonized routes
VAGINAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		ABC Balance Cure	openfda.brand_name
generic name		QUERCUS ACUTISSIMA SAP	openfda.generic_name
manufacturer name		ABCPharm co.,LTD	openfda.manufacturer_name
ndc	package	87368-0001-1	openfda.package_ndc
ndc	product	87368-0001	openfda.product_ndc
ndc11	package	87368000101	derived:openfda.package_ndc
spl id		49e26874-0058-7724-e063-6294a90a0fa8	id
spl set id		49d159e9-b532-7b8b-e063-6394a90a3712	set_id
unii		0TVP714IPW	openfda.unii

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

∙Do not use this product for any purpose other than vaginal cleansing. ∙Do not use this product in the eyes, nose, ears, mouth, or anus. ∙This product is single-use only. Do not reuse. ∙Read the instructions before use, and if any abnormalities occur during use, stop immediately and consult a healthcare professional.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.