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#
Contacts and useful links#
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
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 | Effective |
|---|---|---|---|
| 79c101e4-e5e3-43d7-be20-f7477d1e7556 | Product name | 1 | 20241230 |
| 34b7b043-6d89-4d95-9bed-7f5f2b49e6ef | Product name | 2 | 20200325 |
| 37e0ae3d-ccb0-0ec8-fae8-e1f0917a8a04 | Product name | 2 | 20200325 |
| 739a54c2-5f56-495a-aa67-4295fbc1cc86 | Product name | 2 | 20200325 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43853-0023-1 | HGH | 30 mL in 1 BOTTLE | LIQUID | 30 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 43853-0023 | HGH (HUMAN GROWTH HORMONE) LIQUID [PROBLEN] | 4 | Current NDC, Legacy NDC, 1 package rows | 20221201_3eacca8a-fefe-4ef1-b74d-e51e1024a991.zip |
Products#
Every source-derived product name is available through these pages.
- HGH
- Human growth hormone
- ALCOHOL
- WATER
- SOMATROPIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 43853-0023 | 43853-0023-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | IACT |
| WATER | 059QF0KO0R | IACT |
| SOMATROPIN | NQX9KB6PCL | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| HGH | HUMAN GROWTH HORMONE | ProBLEN | 3eacca8a-fefe-4ef1-b74d-e51e1024a991 | 2022-11-30 | Warnings | 43853-0023-1 43853-0023 43853002301 eeb420f0-c924-0d96-e053-2a95a90afe36 3eacca8a-fefe-4ef1-b74d-e51e1024a991 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
