HGH

Manufacturer
ProBLEN
Effective date
2022-11-30
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:18:39

Label at a glance#

ProductHGH
Active ingredientSOMATROPIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients - Equal Amounts Of:
Human Growth Hormone 30X, Liver Extract 6X, Pituitary Extract 30X.

* Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated

INDICATIONS & USAGE SECTION

Uses: Temporarily supports the body to rebalance Human Growth Hormone (HGH) output. Symptoms of imbalanced HGH may include: poor muscle/fat balance, dry wrinkled-looking skin, low energy, sleeplessness, weak immune system.*

WARNINGS SECTION

Warnings:
Not for use on children. If symptoms continue to recur, or if sleeplessness persists continuously for more than two weeks, consult a physician. As with all medicines, if you are pregnant or breast feeding, consult a health professional before using this product. Keep out of the reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions: Adults: Hold the spray-top close to your open mouth and spray twice directly under your tongue, three times a day. Some people notice improvement within two or three weeks, others take longer.

OTHER SAFETY INFORMATION

Other Information: Store at room temperature.

Tamper Evident: There is a seal around the entire bottle. Do not use if this seal is broken or missing.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic Ethanol, Purified Water.

OTC - QUESTIONS SECTION

Distributed By: ProBLEN (888) 326-2121 3021 Ridge Rd., Rockwall, TX 75032
Questions or Comments: www.problen.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 43853-0023-1

HGH 

HOMEOPATHIC 

ORGANOTHERAPY

1.0 FL OZ (30mL) 20% ALCOHOL

prOBLENopathy

1 oz. bottle label1 oz. bottle label

OTC - PURPOSE SECTION

Temporarily supports the body to rebalance Human Growth Hormone (HGH) output. Symptoms of imbalanced HGH may include: poor muscle/fat balance, dry wrinkled-looking skin, low energy, sleeplessness, weak immune system.*

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
43853-0023-1HGH30 mL in 1 BOTTLELIQUID304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43853-0023HGH (HUMAN GROWTH HORMONE) LIQUID [PROBLEN]4Current NDC, Legacy NDC, 1 package rows20221201_3eacca8a-fefe-4ef1-b74d-e51e1024a991.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43853-002343853-0023-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
SOMATROPINNQX9KB6PCLACTIB

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
HGHHUMAN GROWTH HORMONEProBLEN3eacca8a-fefe-4ef1-b74d-e51e1024a9912022-11-30WarningsExact identifier
ndc (package): 43853-0023-1
ndc (product): 43853-0023
ndc11 (package): 43853002301
spl id: eeb420f0-c924-0d96-e053-2a95a90afe36
spl set id: 3eacca8a-fefe-4ef1-b74d-e51e1024a991

Reported adverse events (FAERS/openFDA)#

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