NDC 65121-887

Pain Away Solution

Aconitum Nepellus Hypericum Peforatum Lycopodium Clavatum Phosphorus Rhus Toxicodendron Secale Cornutum

Pain Away Solution is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Pure Source, Llc. The primary component is Hypericum Perforatum; Lycopodium Clavatum Spore; Aconitum Napellus; Phosphorus; Toxicodendron Pubescens Leaf; Claviceps Purpurea Sclerotium.

Product ID65121-887_579b1f76-1298-684f-e053-2a91aa0a83d7
NDC65121-887
Product TypeHuman Otc Drug
Proprietary NamePain Away Solution
Generic NameAconitum Nepellus Hypericum Peforatum Lycopodium Clavatum Phosphorus Rhus Toxicodendron Secale Cornutum
Dosage FormSpray
Route of AdministrationTOPICAL
Marketing Start Date2017-08-25
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NamePure Source, LLC
Substance NameHYPERICUM PERFORATUM; LYCOPODIUM CLAVATUM SPORE; ACONITUM NAPELLUS; PHOSPHORUS; TOXICODENDRON PUBESCENS LEAF; CLAVICEPS PURPUREA SCLEROTIUM
Active Ingredient Strength24 [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 65121-887-01

10 mL in 1 BOTTLE, GLASS (65121-887-01)
Marketing Start Date2017-08-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 65121-887-03 [65121088703]

Pain Away Solution SPRAY
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-08-25

NDC 65121-887-02 [65121088702]

Pain Away Solution SPRAY
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-08-25

NDC 65121-887-01 [65121088701]

Pain Away Solution SPRAY
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-08-25

Drug Details

Active Ingredients

IngredientStrength
HYPERICUM PERFORATUM24 [hp_X]/100mL

OpenFDA Data

SPL SET ID:579b1f76-1297-684f-e053-2a91aa0a83d7
Manufacturer
UNII

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