HGH-Pro

Manufacturer
Guangzhou Renuma Medical Systems Co., Ltd | Apotheca Company
Effective date
2017-10-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:57

Label at a glance#

ProductHGH-Pro T020
Active ingredientSOMATROPIN, SUS SCROFA PITUITARY GLAND, PORK LIVER
Label structure9 sections

Indications and uses

May temporarily relieve some of the symptoms of aging and/or run-down condition, which may include: low energy, lack of vigor and sleeplessness.

Dosage and administration

Adults only: 7 drops 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Human Growth Hormone 30X (2 Parts), Hypophysis Suis 30X (2 Parts), Hepar Suis 6X (1 Part).

USES:

OTC - PURPOSE SECTION

May temporarily relieve some of the symptoms of aging and/or run-down condition, which may include: low energy, lack of vigor and sleeplessness.

WARNINGS:

WARNINGS SECTION

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:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults only: 7 drops 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional.

USES:

INDICATIONS & USAGE SECTION

May temporarily relieve some of the symptoms of aging and/or run-down condition, which may include: low energy, lack of vigor and sleeplessness.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, Glycerin.

QUESTIONS:

OTC - QUESTIONS SECTION

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:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HGH-PRO
T020
HOMEOPATHIC
2 fl. oz. (59 ml)

HGH-ProHGH-Pro

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
79c101e4-e5e3-43d7-be20-f7477d1e7556Product name120241230
34b7b043-6d89-4d95-9bed-7f5f2b49e6efProduct name220200325
37e0ae3d-ccb0-0ec8-fae8-e1f0917a8a04Product name220200325
739a54c2-5f56-495a-aa67-4295fbc1cc86Product name220200325

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71742-0014-1HGH-ProT02059 mL in 1 PACKAGELIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71742-0014HGH-PRO T020 (HUMAN GROWTH HORMONE, HYPOPHYSIS SUIS, HEPAR SUIS) LIQUID [GUANGZHOU RENUMA MEDICAL SYSTEMS CO., LTD]1Current NDC, Legacy NDC, 1 package rows20171101_ec7e7b1b-9b57-4fa2-8017-23e9ec2d1478.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71742-001471742-0014-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
HGH-Pro T020HUMAN GROWTH HORMONE, HYPOPHYSIS SUIS, HEPAR SUISGuangzhou Renuma Medical Systems Co., Ltdec7e7b1b-9b57-4fa2-8017-23e9ec2d14782017-10-31WarningsExact identifier
ndc (package): 71742-0014-1
ndc (product): 71742-0014
ndc11 (package): 71742001401
spl id: a7260dff-03f1-4824-bdff-1359f37b58f2
spl set id: ec7e7b1b-9b57-4fa2-8017-23e9ec2d1478

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.