GH
GH is an FDA drug label for the active ingredient HUMAN GROWTH HORMONE, PITUITARIA GLANDULA, HEPAR SUIS manufactured by Oxylife Nutritional Supplements Inc administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260513.
- Generic name
- HUMAN GROWTH HORMONE, PITUITARIA GLANDULA, HEPAR SUIS
- Manufacturer
- Oxylife Nutritional Supplements Inc
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 49295-0001
- Application
- N/A
- Label effective
- 20260513
About this product
GH is an FDA-registered drug product whose active ingredient is HUMAN GROWTH HORMONE, PITUITARIA GLANDULA, HEPAR SUIS. It is labelled by Oxylife Nutritional Supplements Inc taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 49295-0001, label effective 20260513. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing HUMAN GROWTH HORMONE, PITUITARIA GLANDULA, HEPAR SUIS are most often described in connection with: temporary relief, symptoms aging, run-down condition, include low, energy lack, vigor sleeplessness. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
INDICATIONS: For temporary relief of some of the symptoms of aging and/or a run-down condition, which may include: low energy, lack of vigor, sleeplessness.
Dosage & Administration
DIRECTIONS: Adults Only: Spray twice under the tongue three times a day. This bottle contains about a 1 month supply. Some notice improvement within 2 to 3 weeks, others longer.
Warnings
WARNINGS: Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if symptoms persist, worsen or if new symptoms occur. If pregnant or breast-feeding, consult a health professional before use. FOR YOUR PROTECTION, THERE IS A SEAL AROUND THE NECK OF THE BOTTLE. DO NOT USE IF SEAL IS BROKEN OR MISSING.
Recall and safety notices
5 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.
| Recall | Product | Firm | Class | Status | Reported |
|---|---|---|---|---|---|
| D-0009-2027 | Sterile High Performance Ultra Lubricating Eye Drops (Polyethylene Glycol 400, 0.4% Relieves Dry and Irritated Eyes) Product size: 0.5 fl oz (15 mL); a) LEADER, DISTRIBUTED BY CARDINAL HEALTH, DUBLIN, OHIO 43017, www.myleader.com, NDC 70000-0457-1; b) exchange select, Manufactured for your Military Exchange By: K.C Pharmaceuticals, Inc., Pomona, CA 9176, UPC: 6 1429905619 0; c) Good Sense, Distributed By: Perrigo Direct Inc., Peachtree City, GA 30269, NDC 50804-160-01; d) Walgreens, DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD, DEERFIELD, IL 60015, UPC 3 11917 20167 2. | K.C. Pharmaceuticals, Inc. | Class II | Ongoing | 20261014 |
| D-0002-2027 | Artificial Tears Sterile Lubricant Eye Drops (polyvinyl alcohol 0.5%, povidone 0.6%), 0.5 FL OZ (15 mL) bottles; a) Best Choice, PROUDLY DISTRIBUTED BY: VALU MERCHANDISERS, CO., 5000 KANSAS CITY, KS 66106, UPC 0 70038 47008 3; b) LEADER, DISTRIBUTED BY CARDINAL HEALTH, DUBLIN, OHIO 43017, www.myleader.com, NDC 70000-0011-1; c) Good Neighbor Pharmacy, Distributed By AmerisourceBergen, 1 West First Avenue, Conshohocken, PA 19428, NDC 24385-006-05; d) Good Sense, Distributed By: Geiss, Destin& Dunn, Inc., A Perrigo Company, Peachtree City, GA 30269, NDC 50804-110-01; e) Medic'c Choice, Sterile 0.5 fl. oz. (15 mL), Manufactured by KC Pharmaceuticals, Inc., Pomona, CA 91768, NDC 55651-008-01; f) P, DISTRIBUTED BY PUBLIX SUPER MARKETS, INC, LAKELAND, FL 33811, UPC 0 41415 00976 9; g) Quality Choice, Distributed by CDMA Inc, Novi, MI NDC 83324-189-14; h) TopCare health, DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELKGROVE VILLAGE, IL 60007, UPC 0 36800 09331 7; I) Walgreens, DISTRIBUTED BY: WALGREEN CO. DEERFIELD, IL 60015, UPC 3 11917 06503 8; J) Kroger, DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202, UPC 0 11110 38600 7. | K.C. Pharmaceuticals, Inc. | Class II | Ongoing | 20261014 |
| D-0861-2026 | Major LubriFresh P.M. Nighttime Ointment, Net wt. 0.125 oz. (3.5 g) tubes, Distributed by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152, NDC 0904-6488-38 | Sterling Pharmaceutical Services LLC | Class II | Ongoing | 20260930 |
| D-0778-2026 | Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 1000-count bottles, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India, NDC 16729-450-17. | ACCORD HEALTHCARE, INC. | Class II | Ongoing | 20260902 |
| D-0782-2026 | Levothyroxine Sodium Tablets, USP, 137 mcg (0.137 mg), packaged in a) 90-count bottles (NDC 16729-454-15) b) 1000-count bottles (NDC 16729-454-17), Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India. | ACCORD HEALTHCARE, INC. | Class II | Ongoing | 20260902 |
Frequently asked questions
What is GH used for?
INDICATIONS: For temporary relief of some of the symptoms of aging and/or a run-down condition, which may include: low energy, lack of vigor, sleeplessness.
Who makes GH?
Oxylife Nutritional Supplements Inc is the labeler of record for GH.
What form does GH come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is GH prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has GH been recalled?
5 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.