Sunshine MenopauseRelief

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: Sunshine MenopauseRelief
Generic name: MENOPAUSE SUPPOSITORY
Manufacturer: Apcco Labs, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 37de2698-c6ae-ab67-e063-6394a90ab248
SPL ID: 37de2698-c6ad-ab67-e063-6394a90ab248
Version: 1
Effective date: 2025-06-18
Source export date: 2026-10-12
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/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:31:34

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Sunshine MenopauseRelief	openfda.brand_name
generic name		MENOPAUSE SUPPOSITORY	openfda.generic_name
manufacturer name		Apcco Labs, Inc	openfda.manufacturer_name
ndc	package	82126-002-30	openfda.package_ndc
ndc	product	82126-002	openfda.product_ndc
ndc11	package	82126000230	derived:openfda.package_ndc
spl id		37de2698-c6ad-ab67-e063-6394a90ab248	id
spl set id		37de2698-c6ae-ab67-e063-6394a90ab248	set_id
unii		O80TY208ZW	openfda.unii
unii		G7W43U4YTF	openfda.unii
unii		K73E24S6X9	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

WARNINGS: Warnings For vaginal use only. Not for oral consumption. Do not use If you are allergic to any of the ingredients. When using this product do not exceed the recommended dose. Ask a doctor before use If you have irregular menstrual cycles not related to menopause • If you are taking hormone replacement therapy (HRT) or other medications Stop use and ask a doctor If symptoms persist for more than 7 days or worsen If new symptoms occur If you experience an allergic reaction

Reported adverse events (FAERS/openFDA)#

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