Menopause Liquid
Product Images NDC 50845-0092

2 FDA label images from Liddell Laboratories, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Menopause (NDC 50845-0092). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Liddell Laboratories, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Menopause Ctn (Lidl02 Menopause Ctn 4 11 16)

Menopause Ctn (Lidl02 Menopause Ctn 4 11 16)
Liddell Laboratories Menopause oral spray with Black Cohosh, a homeopathic liquid product in a 1 fl oz (30 ml) bottle containing 20% organic alcohol. The label highlights its use for menopausal symptoms such as hormonal imbalance, emotional fluctuations, hot flashes, and irritability, and includes directions for adults to spray twice under the tongue three times a day. The product is made in the USA by Liddell Laboratories, Inc.*
FDA Label Image

Menopause Lbl (Lidl02 Menopause Lbl 4 6 17)

Menopause Lbl (Lidl02 Menopause Lbl 4 6 17)
The label of Liddell Laboratories' Menopause oral spray homeopathic liquid features the product abbreviation 'Mp' prominently with 'Menopause with Black Cohosh' indicated. The 1.0 FL OZ (30 ml) bottle contains 20% organic alcohol. Ingredients include Agnus Castus, Angelica Sinensis, Apis Mellifica, Aralia Quinquefolia, Arnica Montana, Cimicifuga Racemosa, Galium Aparine, Glycyrrhiza Glabra, Oophorinum Suis, Sepia, Thuja Occidentalis, and Viscum Album at various potencies. The label includes directions for adults to spray twice under the tongue three times daily and a warning about tamper evidence on the bottle.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.