Label: GH- human growth hormone, pituitaria glandula, hepar suis spray
- NDC Code(s): 49295-0001-1
- Packager: Oxylife Nutritional Supplements Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated September 28, 2017
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS:
- INDICATIONS:
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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.
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- INDICATIONS:
- INACTIVE INGREDIENTS:
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QUESTIONS:
:Distributed by:
OxyLife Nutritional Supplements Inc.
P.O. Box 6451
Chula Vista, CA 91909
Toll Free: 877-982-9800 www.oxylifeco.com
Made in USA with foreign and U.S. components
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
GH
human growth hormone, pituitaria glandula, hepar suis sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49295-0001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SOMATROPIN (UNII: NQX9KB6PCL) (SOMATROPIN - UNII:NQX9KB6PCL) SOMATROPIN 30 [hp_X] in 1 mL SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T) (SUS SCROFA PITUITARY GLAND - UNII:E8S87O660T) SUS SCROFA PITUITARY GLAND 30 [hp_X] in 1 mL PORK LIVER (UNII: 6EC706HI7F) (PORK LIVER - UNII:6EC706HI7F) PORK LIVER 6 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49295-0001-1 60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/14/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/14/2014 Labeler - Oxylife Nutritional Supplements Inc (004341775) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(49295-0001) , api manufacture(49295-0001) , label(49295-0001) , pack(49295-0001)