NDC 53346-1314

DR. RECKEWEG R14 Quieta Combination Product

Ammonium Bromatum 3x, Avena Sativa 1x, Chamomilla 4x, Coffea Cruda 4x, Eschscholtzia Californica 2x, Humulus Lupulus 2x, Ignatia Amara 6x, Passiflora Incarnata 2x, Valeriana Officinalis 1x, Zincum Valerianicum 6x

DR. RECKEWEG R14 Quieta Combination Product is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Pharmazeutische Fabrik Dr. Reckeweg & Co. The primary component is Ammonium Bromide; Avena Sativa Flowering Top; Matricaria Recutita; Arabica Coffee Bean; Eschscholzia Californica Flowering Top; Hops; Strychnos Ignatii Seed; Passiflora Incarnata Flowering Top; Valerian; Zinc Valerate Dihydrate.

Product ID53346-1314_b3f078a8-34d3-4202-8f73-7450a1b31fd6
NDC53346-1314
Product TypeHuman Otc Drug
Proprietary NameDR. RECKEWEG R14 Quieta Combination Product
Generic NameAmmonium Bromatum 3x, Avena Sativa 1x, Chamomilla 4x, Coffea Cruda 4x, Eschscholtzia Californica 2x, Humulus Lupulus 2x, Ignatia Amara 6x, Passiflora Incarnata 2x, Valeriana Officinalis 1x, Zincum Valerianicum 6x
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date1986-06-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NamePHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO
Substance NameAMMONIUM BROMIDE; AVENA SATIVA FLOWERING TOP; MATRICARIA RECUTITA; ARABICA COFFEE BEAN; ESCHSCHOLZIA CALIFORNICA FLOWERING TOP; HOPS; STRYCHNOS IGNATII SEED; PASSIFLORA INCARNATA FLOWERING TOP; VALERIAN; ZINC VALERATE DIHYDRATE
Active Ingredient Strength3 [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 53346-1314-5

50 mL in 1 BOTTLE (53346-1314-5)
Marketing Start Date1986-06-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 53346-1314-5 [53346131405]

DR. RECKEWEG R14 Quieta Combination Product LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1986-06-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
AMMONIUM BROMIDE3 [hp_X]/50mL

OpenFDA Data

SPL SET ID:b4cba022-c38c-4308-9be6-8eb99e6aacbd
Manufacturer
UNII
UPC Code
  • 0669330000359

  • © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.