NDC 71919-197

Chrysarobinum

Chrysarobin

Chrysarobinum is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Chrysarobin.

Product ID71919-197_7e468dc6-44be-b3be-e053-2a91aa0ad344
NDC71919-197
Product TypeHuman Otc Drug
Proprietary NameChrysarobinum
Generic NameChrysarobin
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2011-03-07
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameWashington Homeopathic Products
Substance NameCHRYSAROBIN
Active Ingredient Strength30 [hp_C]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71919-197-07

15 mL in 1 VIAL, GLASS (71919-197-07)
Marketing Start Date2011-03-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71919-197-08 [71919019708]

Chrysarobinum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-03-07

NDC 71919-197-09 [71919019709]

Chrysarobinum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-03-07

NDC 71919-197-10 [71919019710]

Chrysarobinum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-03-07

NDC 71919-197-07 [71919019707]

Chrysarobinum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-03-07

Drug Details

Active Ingredients

IngredientStrength
CHRYSAROBIN30 [hp_C]/mL

OpenFDA Data

SPL SET ID:0d2472c9-b393-44ee-8d48-35bd8d70dcfc
Manufacturer
UNII
UPC Code
  • 0740640279021
  • NDC Crossover Matching brand name "Chrysarobinum" or generic name "Chrysarobin"

    NDCBrand NameGeneric Name
    68428-316ChrysarobinumCHRYSAROBIN
    71919-197ChrysarobinumCHRYSAROBIN

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