Label: DERMATROPIN- transdermal hgh gel gel

  • NDC Code(s): 69953-318-01
  • Packager: Rapha Pharmaceuticals, 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 April 6, 2019

If you are a consumer or patient please visit this version.

  • Active Ingredients

    Somatropin 12X

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  • Purpose

    Dermatropin™ HGH Transdermal Gel helps promotre brighter, youthful looking skin and may reduce wrinkles. HGH helps speed up healing, repair muscle tissue after exercise, build muscle, boost the immune system, burn fat and improve sleep.*

    *These statements have not been evaluated by the FDA.

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  • Directions

    Apply 2 full pumps in the morning and 2 full pumps in the evening; 5 days on, 2 days off. For intensive use, apply 2 full pumps three times a day.

    • Gel should always be applied to thin areas of the skin where veins are visible.
    • You may apply the gel to your face, wrists, underarms, forearms or behind the knees. Application sites should be rotated.
    • If pregnant or breast feeding, ask a health care professional before use.
    • FOR EXTERNAL USE ONLY
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  • Inactive Ingredients

    Purified Water, Organic Coconut Oil, Absorbic Acid (Vitamin C), Allyl Pentaerythritol Crosspolymer, Organic Aloe Vera (Leaf Juice), Benzyl Alcohol.

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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. (1-800-222-1222)

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  • Package Label Display

    Dermatropin™
    HGH Transdermal Gel

    Anti-Aging
    Human Growth Hormone

    Maximum Strength
    Homeopathic
    Pharmaceutical Grade

    Net. Wt. 5oz. (142g)

    www.buydermatropin.com

    Package Label Display

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  • INGREDIENTS AND APPEARANCE
    DERMATROPIN 
    transdermal hgh gel gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:69953-318
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SOMATROPIN (UNII: NQX9KB6PCL) (SOMATROPIN - UNII:NQX9KB6PCL) SOMATROPIN 12 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    COCONUT OIL (UNII: Q9L0O73W7L)  
    CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:69953-318-01 142 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/25/2019
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 04/25/2019
    Labeler - Rapha Pharmaceuticals, Inc. (079804155)
    Registrant - Rapha Pharmaceuticals, Inc. (079804155)
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