Menopause Relief

Product NDC
57955-7006
11-digit product format
579557006
Labeler code
57955
Product ID
57955-7006_b8e7765b-0eca-4404-818d-9e1cdcca1988
Type
HUMAN OTC DRUG
Nonproprietary name
Amyl nitrosum, Calcarea carbonica, Caulophyllum thalictroides, Cimicifuga racemosa, Ferrum metallicum, Gelsemium sempervirens, Lachesis mutus, Pulsatilla, Sanguinaria canadensis, Sepia, Sulphur, Sulphuricum acidum.
Dosage form
LIQUID
Route
ORAL
Labeler
King Bio Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-06-12
Marketing end
0000-00-00
Substance
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
Active strength
10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
57955-7006-2579557006021 BOTTLE, SPRAY in 1 CARTON (57955-7006-2) > 59 mL in 1 BOTTLE, SPRAY2022-06-120000-00-00NoNoCurrent