Search by Drug Name or NDC

NDC 71742-0004-01 Female Vitality 12; 3; 3; 12; 12; 12; 12; 6; 6; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL Details

Female Vitality 12; 3; 3; 12; 12; 12; 12; 6; 6; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

Female Vitality is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Guangzhou Renuma Medical Systems Co., Ltd. The primary component is ANEMONE PRATENSIS; BLACK COHOSH; FUCUS VESICULOSUS; GRAPHITE; LACHESIS MUTA VENOM; SEPIA OFFICINALIS JUICE; SODIUM CHLORIDE; SUS SCROFA OVARY; SUS SCROFA PITUITARY GLAND; SUS SCROFA THYROID.

Product Information

NDC	71742-0004
Product ID	71742-0004_e568062e-50f9-4442-904a-72e7f33da401
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	Female Vitality
Proprietary Name Suffix	T010
Non-Proprietary Name	Cimicifuga Racemosa, Fucus Vesiculosus, Oophorinum (Suis), Hypophysis Suis, Thyroidinum (Suis), Graphites, Lachesis Mutus, Natrum Muriaticum, Pulsatilla (Pratensis), Sepia
Product Type	HUMAN OTC DRUG
Dosage Form	LIQUID
Route	ORAL
Active Ingredient Strength	12; 3; 3; 12; 12; 12; 12; 6; 6; 6
Active Ingredient Units	[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Substance Name	ANEMONE PRATENSIS; BLACK COHOSH; FUCUS VESICULOSUS; GRAPHITE; LACHESIS MUTA VENOM; SEPIA OFFICINALIS JUICE; SODIUM CHLORIDE; SUS SCROFA OVARY; SUS SCROFA PITUITARY GLAND; SUS SCROFA THYROID
Labeler Name	Guangzhou Renuma Medical Systems Co., Ltd
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	UNAPPROVED HOMEOPATHIC
Application Number	n/a
Listing Certified Through	2024-12-31

Package

Package Images

NDC 71742-0004-01 (71742000401)

Pricing Information	N/A
NDC Package Code	71742-0004-1
Billing NDC	71742000401
Package	59 mL in 1 BOTTLE, DROPPER (71742-0004-1)
Marketing Start Date	2017-10-20
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 694f0c36-b656-471a-9f38-2efb5193e05a Details

ACTIVE INGREDIENTS:

Cimicifuga Racemosa 3X, Fucus Vesiculosus 3X, Oophorinum (Suis) 6X, Pituitaria Glandula (Suis) 6X, Thyroidinum (Suis) 6X, Graphites 12X, Lachesis Mutus 12X, Natrum Muriaticum 12X, Pulsatilla (Pratensis) 12X, Sepia 12X.

INDICATIONS:

May temporarily relieve menstrual pain and cramps, pain immediately prior to menses, sore breasts associated with menstruation.

WARNINGS:

If pregnant or breast-feeding, ask a health 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 tamper evident seal is broken or missing. Store in a cool, dry place.

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:

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

May temporarily relieve menstrual pain and cramps, pain immediately prior to menses, sore breasts associated with menstruation.

INACTIVE INGREDIENTS:

Demineralized water, Glycerin.

QUESTIONS:

Distributed by:

Guangzhou Renuma Medical

Systems Co., Ltd.

No. 5, 2nd Floor, Ascendas 2nd Street

Sino-Singapore Guangzhou Knowledge City

Guangzhou 510555, China

PACKAGE LABEL DISPLAY:

FEMALE

VITALITY

T010

HOMEOPATHIC

2 fl. oz. (59 ml)

INGREDIENTS AND APPEARANCE

FEMALE VITALITY T010

cimicifuga racemosa, fucus vesiculosus, oophorinum (suis), hypophysis suis, thyroidinum (suis), graphites, lachesis mutus, natrum muriaticum, pulsatilla (pratensis), sepia liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71742-0004
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BLACK COHOSH (UNII: K73E24S6X9) (BLACK COHOSH - UNII:K73E24S6X9)	BLACK COHOSH	3 [hp_X] in 1 mL
FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M)	FUCUS VESICULOSUS	3 [hp_X] in 1 mL
SUS SCROFA OVARY (UNII: S7YTV04R8O) (SUS SCROFA OVARY - UNII:S7YTV04R8O)	SUS SCROFA OVARY	6 [hp_X] in 1 mL
SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T) (SUS SCROFA PITUITARY GLAND - UNII:E8S87O660T)	SUS SCROFA PITUITARY GLAND	6 [hp_X] in 1 mL
SUS SCROFA THYROID (UNII: 6RV024OAUQ) (SUS SCROFA THYROID - UNII:6RV024OAUQ)	SUS SCROFA THYROID	6 [hp_X] in 1 mL
GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O)	GRAPHITE	12 [hp_X] in 1 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	12 [hp_X] in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	12 [hp_X] in 1 mL
ANEMONE PRATENSIS (UNII: 8E272251DI) (ANEMONE PRATENSIS - UNII:8E272251DI)	ANEMONE PRATENSIS	12 [hp_X] in 1 mL
SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2)	SEPIA OFFICINALIS JUICE	12 [hp_X] 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:71742-0004-1	59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	10/20/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		10/20/2017

Labeler - Guangzhou Renuma Medical Systems Co., Ltd (544538706)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(71742-0004) , api manufacture(71742-0004) , label(71742-0004) , pack(71742-0004)

Revised: 10/2017

Document Id: e568062e-50f9-4442-904a-72e7f33da401

Set id: 694f0c36-b656-471a-9f38-2efb5193e05a

Version: 1

Effective Time: 20171020

Search by Drug Name or NDC

NDC 71742-0004-01 Female Vitality 12; 3; 3; 12; 12; 12; 12; 6; 6; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL Details

Female Vitality 12; 3; 3; 12; 12; 12; 12; 6; 6; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

Product Information

Package

Package Images

NDC 71742-0004-01 (71742000401)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 694f0c36-b656-471a-9f38-2efb5193e05a Details

ACTIVE INGREDIENTS:

INDICATIONS:

WARNINGS:

KEEP OUT OF REACH OF CHILDREN:

DIRECTIONS:

INDICATIONS:

INACTIVE INGREDIENTS:

QUESTIONS:

PACKAGE LABEL DISPLAY:

INGREDIENTS AND APPEARANCE

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