Search by Drug Name or NDC

NDC 71742-0009-01 Glucose Control 12; 6; 9; 12; 12; 12; 6; 6; 6; 3; 12 [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; [hp_X]/mL Details

Glucose Control 12; 6; 9; 12; 12; 12; 6; 6; 6; 3; 12 [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; [hp_X]/mL

Glucose Control 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 ACETIC ACID; GOLDENSEAL; KIDNEY BEAN; LACTIC ACID; PHOSPHORIC ACID; PHOSPHORUS; SUS SCROFA ADRENAL GLAND; SUS SCROFA PANCREAS; SUS SCROFA PITUITARY GLAND; SYZYGIUM CUMINI SEED; URANYL NITRATE HEXAHYDRATE.

Product Information

NDC	71742-0009
Product ID	71742-0009_5e65d625-8b6c-48af-84c6-f91fdf8cf01d
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	Glucose Control
Proprietary Name Suffix	T015
Non-Proprietary Name	Syzygium Jambolanum, Glandula Suprarenalis Suis, Hydrastis Canadensis, Hypophysis Suis, Pancreas Suis, Phaseolus, Aceticum Acidum, Lacticum Acidum, Phosphoricum Acidum, Phosphorus, Uranium Nitricum
Product Type	HUMAN OTC DRUG
Dosage Form	LIQUID
Route	ORAL
Active Ingredient Strength	12; 6; 9; 12; 12; 12; 6; 6; 6; 3; 12
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; [hp_X]/mL
Substance Name	ACETIC ACID; GOLDENSEAL; KIDNEY BEAN; LACTIC ACID; PHOSPHORIC ACID; PHOSPHORUS; SUS SCROFA ADRENAL GLAND; SUS SCROFA PANCREAS; SUS SCROFA PITUITARY GLAND; SYZYGIUM CUMINI SEED; URANYL NITRATE HEXAHYDRATE
Labeler Name	Guangzhou Renuma Medical Systems Co., Ltd
Pharmaceutical Class	Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS]
DEA Schedule	n/a
Marketing Category	UNAPPROVED HOMEOPATHIC
Application Number	n/a
Listing Certified Through	2024-12-31

Package

Package Images

NDC 71742-0009-01 (71742000901)

Pricing Information	N/A
NDC Package Code	71742-0009-1
Billing NDC	71742000901
Package	59 mL in 1 BOTTLE, DROPPER (71742-0009-1)
Marketing Start Date	2017-10-26
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 3fd02c0a-5cf1-4f35-86d0-d5d09e63f39b Details

ACTIVE INGREDIENTS:

Syzygium Jambolanum 3X, Glandula Suprarenalis Suis 6X, Hydrastis Canadensis 3X, Hypophysis Suis 6X, Pancreas Suis 6X, Phaseolus 9X, Aceticum Acidum 12X, Lacticum Acidum 12X, Phosphoricum Acidum 12X, Phosphorus 12X, Uranium Nitricum 12X.

INDICATIONS:

Pancreas support, blood sugar regulation.

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 tamper evident seal is broken or missing.

Store in 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:

Pancreas support, blood sugar regulation.

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:

GLUCOSE

CONTROL

T015

HOMEOPATHIC

2 fl. oz. (59 ml)

INGREDIENTS AND APPEARANCE

GLUCOSE CONTROL T015

syzygium jambolanum, glandula suprarenalis suis, hydrastis canadensis, hypophysis suis, pancreas suis, phaseolus, aceticum acidum, lacticum acidum, phosphoricum acidum, phosphorus, uranium nitricum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71742-0009
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SYZYGIUM CUMINI SEED (UNII: 820LSF646I) (SYZYGIUM CUMINI SEED - UNII:820LSF646I)	SYZYGIUM CUMINI SEED	3 [hp_X] in 1 mL
SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV)	SUS SCROFA ADRENAL GLAND	6 [hp_X] in 1 mL
GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV)	GOLDENSEAL	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 PANCREAS (UNII: 9Y3J3362RY) (SUS SCROFA PANCREAS - UNII:9Y3J3362RY)	SUS SCROFA PANCREAS	6 [hp_X] in 1 mL
KIDNEY BEAN (UNII: M98C8416QO) (KIDNEY BEAN - UNII:M98C8416QO)	KIDNEY BEAN	9 [hp_X] in 1 mL
ACETIC ACID (UNII: Q40Q9N063P) (ACETIC ACID - UNII:Q40Q9N063P)	ACETIC ACID	12 [hp_X] in 1 mL
LACTIC ACID (UNII: 33X04XA5AT) (LACTIC ACID - UNII:33X04XA5AT)	LACTIC ACID	12 [hp_X] in 1 mL
PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN)	PHOSPHORIC ACID	12 [hp_X] in 1 mL
PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W)	PHOSPHORUS	12 [hp_X] in 1 mL
URANYL NITRATE HEXAHYDRATE (UNII: 3V057702FY) (URANIUM CATION (6+) - UNII:5PI36AS4G7)	URANYL NITRATE HEXAHYDRATE	12 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71742-0009-1	59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	10/26/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		10/26/2017

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

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(71742-0009) , api manufacture(71742-0009) , label(71742-0009) , pack(71742-0009)

Revised: 10/2017

Document Id: 5e65d625-8b6c-48af-84c6-f91fdf8cf01d

Set id: 3fd02c0a-5cf1-4f35-86d0-d5d09e63f39b

Version: 1

Effective Time: 20171026

Search by Drug Name or NDC

NDC 71742-0009-01 Glucose Control 12; 6; 9; 12; 12; 12; 6; 6; 6; 3; 12 [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; [hp_X]/mL Details

Glucose Control 12; 6; 9; 12; 12; 12; 6; 6; 6; 3; 12 [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; [hp_X]/mL

Product Information

Package

Package Images

NDC 71742-0009-01 (71742000901)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 3fd02c0a-5cf1-4f35-86d0-d5d09e63f39b 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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