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.
Updated April 6, 2019
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- Active Ingredients
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.
- Inactive Ingredients
- Package Label Display
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)