Menopause Relief Liquid
NDC Package 57955-9973-2
Package Information
Menopause Relief (amyl nit, calc carb, caulophyllum, cimicifuga, ferrum met, gelsemium, lachesis, pulsatilla, sanguinaria, sepia, sulphur and sulphuricum ac.) liquids is uses † For temporary relief of discomfortsassociated with menopause:hot flashesnight sweatschillsheadachesuterine crampsmood swingssensitivityirritabilityfatiguepoor memory† Claims based on traditional Homeopathic practice, not accepted medical evidence, notFDA evaluated. This formulation utilizes a liquid delivery system. Marketed by King Bio Inc., this product is identified by NDC 57955-9973.
Identification & Billing
Clinical Specifications
- AMYL NITRITE 10 [hp_X]/59mL
- BLACK COHOSH 10 [hp_X]/59mL
- CAULOPHYLLUM THALICTROIDES ROOT 10 [hp_X]/59mL
- GELSEMIUM SEMPERVIRENS ROOT 10 [hp_X]/59mL
- IRON 10 [hp_X]/59mL
- LACHESIS MUTA VENOM 10 [hp_X]/59mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 10 [hp_X]/59mL
- PULSATILLA VULGARIS WHOLE 10 [hp_X]/59mL
- SANGUINARIA CANADENSIS ROOT 10 [hp_X]/59mL
- SEPIA OFFICINALIS JUICE 10 [hp_X]/59mL
- SULFUR 10 [hp_X]/59mL
- SULFURIC ACID 10 [hp_X]/59mL
Regulatory & Marketing
Hierarchy Structure
- 57955 - King Bio Inc.
- 57955-9973 - Menopause Relief
- 57955-9973-2 - 59 mL in 1 BOTTLE, SPRAY
- 57955-9973 - Menopause Relief
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 57955-9973-2 identifies a specific commercial package of 59 ml in 1 bottle, spray of Menopause Relief, a human over the counter drug labeled by King Bio Inc.. This liquid is formulated for oral use and contains amyl nitrite; black cohosh; caulophyllum thalictroides root; gelsemium sempervirens root; iron; lachesis muta venom; oyster shell calcium carbonate, crude; pulsatilla vulgaris whole; sanguinaria canadensis root; sepia officinalis juice; sulfur; sulfuric acid as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by King Bio Inc. on March 13, 2026. The current certification is valid through December 31, 2027.
How is this King Bio Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 57955997302. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.