Label: DERMATROPIN- transdermal hgh gel gel
- NDC Code(s): 69953-318-01
- Packager: Rapha Pharmaceuticals, Inc.
- Category: HUMAN OTC DRUG LABEL
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.
Updated April 6, 2019
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- Active Ingredients
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.Close
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
- Inactive Ingredients
Purified Water, Organic Coconut Oil, Absorbic Acid (Vitamin C), Allyl Pentaerythritol Crosspolymer, Organic Aloe Vera (Leaf Juice), Benzyl Alcohol.Close
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)
- Package Label Display
HGH Transdermal Gel
Human Growth Hormone
Net. Wt. 5oz. (142g)
- INGREDIENTS AND APPEARANCE
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)