Search by Drug Name or NDC

NDC 50181-0084-01 MBM 13 Female 89; 5; 144; 233; 144; 89; 89; 3; 3; 89; 3 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL Details

MBM 13 Female 89; 5; 144; 233; 144; 89; 89; 3; 3; 89; 3 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL

MBM 13 Female is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by The Wellness Center for Research and Education, Inc.. The primary component is BLACK COHOSH; BOS TAURUS HYPOTHALAMUS; CAUSTICUM; DIBASIC POTASSIUM PHOSPHATE; GRAPHITE; LILIUM LANCIFOLIUM WHOLE FLOWERING; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; SCROPHULARIA NODOSA WHOLE; SULFUR; SUS SCROFA PITUITARY GLAND.

Product Information

NDC	50181-0084
Product ID	50181-0084_ac3d8088-244b-4bd1-8d09-97e5fe2e614f
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	MBM 13 Female
Proprietary Name Suffix	n/a
Non-Proprietary Name	Phytolacca Decandra, Hypophysis (SUIS), Scrophularia Nodosa, Hypothalamus (SUIS), Calcarea Carbonica, Cimicifuga Racemosa, Lilium Tigrinum, Sulphur, Causticum, Graphites, Kali Phosphoricum
Product Type	HUMAN OTC DRUG
Dosage Form	LIQUID
Route	ORAL
Active Ingredient Strength	89; 5; 144; 233; 144; 89; 89; 3; 3; 89; 3
Active Ingredient Units	[hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
Substance Name	BLACK COHOSH; BOS TAURUS HYPOTHALAMUS; CAUSTICUM; DIBASIC POTASSIUM PHOSPHATE; GRAPHITE; LILIUM LANCIFOLIUM WHOLE FLOWERING; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; SCROPHULARIA NODOSA WHOLE; SULFUR; SUS SCROFA PITUITARY GLAND
Labeler Name	The Wellness Center for Research and Education, Inc.
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	UNAPPROVED HOMEOPATHIC
Application Number	n/a
Listing Certified Through	2023-12-31

Package

Package Images

NDC 50181-0084-01 (50181008401)

Pricing Information	N/A
NDC Package Code	50181-0084-1
Billing NDC	50181008401
Package	30 mL in 1 BOTTLE, DROPPER (50181-0084-1)
Marketing Start Date	2022-05-03
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 2ba45d16-58d8-4921-ae06-0cec43238dd3 Details

ACTIVE INGREDIENT:

Phytolacca Decandra 3C, Hypophysis (SUIS) 3C, Scrophularia Nodosa 3C, Hypothalamus (SUIS) 5C, Calcarea Carbonica 89C, Cimicifuga Racemosa 89C, Lilium Tigrinum 89C, Sulphur 89C, Causticum 144C, Graphites 144C, Kali Phosphoricum 233C

INDICATIONS:

For the temporary relief of emotionlessness, denial, numbness, and unresponsiveness.

WARNINGS:

If pregnant or breast-feeding, ask a health care professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

Feel the emotion fully, breathe deeply-connecting breaths. Put 5 drops under tongue to release emotion. Continue 5 drops 2 times daily as needed. Consult a physician for use in children under 12 years of age.

INDICATIONS:

For the temporary relief of emotionlessness, denial, numbness, and unresponsiveness.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol.

QUESTIONS:

MFD FOR:

The Wellness Center for Research and Education, Inc.

1237 S. Victoria Ave. Suite 169

Oxnard, CA 93035

PACKAGE LABEL DISPLAY

NDC: 50181-0084-1

Fibonacci Series

Female

Unresponsive

HOMEOPATHIC

1 fluid oz. (30 ml)

INGREDIENTS AND APPEARANCE

MBM 13 FEMALE

phytolacca decandra, hypophysis (suis), scrophularia nodosa, hypothalamus (suis), calcarea carbonica, cimicifuga racemosa, lilium tigrinum, sulphur, causticum, graphites, kali phosphoricum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50181-0084
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG)	PHYTOLACCA AMERICANA ROOT	3 [hp_C] in 1 mL
SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT) (SUS SCROFA PITUITARY GLAND - UNII:L0PFEMQ1DT)	SUS SCROFA PITUITARY GLAND	3 [hp_C] in 1 mL
SCROPHULARIA NODOSA WHOLE (UNII: 7H443NUB2T) (SCROPHULARIA NODOSA - UNII:7H443NUB2T)	SCROPHULARIA NODOSA WHOLE	3 [hp_C] in 1 mL
BOS TAURUS HYPOTHALAMUS (UNII: S6G2NLH4Y7) (BOS TAURUS HYPOTHALAMUS - UNII:S6G2NLH4Y7)	BOS TAURUS HYPOTHALAMUS	5 [hp_C] in 1 mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I)	OYSTER SHELL CALCIUM CARBONATE, CRUDE	89 [hp_C] in 1 mL
BLACK COHOSH (UNII: K73E24S6X9) (BLACK COHOSH - UNII:K73E24S6X9)	BLACK COHOSH	89 [hp_C] in 1 mL
LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI) (LILIUM LANCIFOLIUM WHOLE FLOWERING - UNII:X67Z2963PI)	LILIUM LANCIFOLIUM WHOLE FLOWERING	89 [hp_C] in 1 mL
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	89 [hp_C] in 1 mL
CAUSTICUM (UNII: DD5FO1WKFU) (CAUSTICUM - UNII:DD5FO1WKFU)	CAUSTICUM	144 [hp_C] in 1 mL
GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O)	GRAPHITE	144 [hp_C] in 1 mL
DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR)	DIBASIC POTASSIUM PHOSPHATE	233 [hp_C] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50181-0084-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	05/03/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		05/03/2022

Labeler - The Wellness Center for Research and Education, Inc. (832363993)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(50181-0084) , api manufacture(50181-0084) , label(50181-0084) , pack(50181-0084)

Revised: 5/2022

Document Id: ac3d8088-244b-4bd1-8d09-97e5fe2e614f

Set id: 2ba45d16-58d8-4921-ae06-0cec43238dd3

Version: 1

Effective Time: 20220503

Search by Drug Name or NDC

NDC 50181-0084-01 MBM 13 Female 89; 5; 144; 233; 144; 89; 89; 3; 3; 89; 3 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL Details

MBM 13 Female 89; 5; 144; 233; 144; 89; 89; 3; 3; 89; 3 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL

Product Information

Package

Package Images

NDC 50181-0084-01 (50181008401)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 2ba45d16-58d8-4921-ae06-0cec43238dd3 Details

ACTIVE INGREDIENT:

INDICATIONS:

WARNINGS:

KEEP OUT OF REACH OF CHILDREN:

DIRECTIONS:

INDICATIONS:

INACTIVE INGREDIENTS:

QUESTIONS:

PACKAGE LABEL DISPLAY

INGREDIENTS AND APPEARANCE

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