NDC 43406-0099

MOTION SICKNESS HP

Arnica Montana, Bryonia Alba Root, Quinine Sulfate, Anamirta Cocculus Seed, Conium Maculatum Flowering Top, Strychnos Ignatii Seed, Ipecac, Potassium Carbonate, Strychnos Nux-vomica Seed, Sepia Officinalis Juice, Tobacco Leaf, Veratrum Album Root

MOTION SICKNESS HP is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Natural Creations, Inc.. The primary component is Arnica Montana; Bryonia Alba Root; Quinine Sulfate; Anamirta Cocculus Seed; Conium Maculatum Flowering Top; Strychnos Ignatii Seed; Ipecac; Potassium Carbonate; Strychnos Nux-vomica Seed; Sepia Officinalis Juice; Tobacco Leaf; Veratrum Album Root.

• Product ID: 43406-0099_40cf4b0e-e82f-449a-bc11-d7c6b9a97664
• NDC: 43406-0099
• Product Type: Human Otc Drug
• Proprietary Name: MOTION SICKNESS HP
• Generic Name: Arnica Montana, Bryonia Alba Root, Quinine Sulfate, Anamirta Cocculus Seed, Conium Maculatum Flowering Top, Strychnos Ignatii Seed, Ipecac, Potassium Carbonate, Strychnos Nux-vomica Seed, Sepia Officinalis Juice, Tobacco Leaf, Veratrum Album Root
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2007-05-29
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Natural Creations, Inc.
• Substance Name: ARNICA MONTANA; BRYONIA ALBA ROOT; QUININE SULFATE; ANAMIRTA COCCULUS SEED; CONIUM MACULATUM FLOWERING TOP; STRYCHNOS IGNATII SEED; IPECAC; POTASSIUM CARBONATE; STRYCHNOS NUX-VOMICA SEED; SEPIA OFFICINALIS JUICE; TOBACCO LEAF; VERATRUM ALBUM ROOT
• Active Ingredient Strength: 30 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 43406-0099-1

30 mL in 1 BOTTLE, DROPPER (43406-0099-1)

• Marketing Start Date: 2007-05-29
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43406-0099-1 [43406009901]

MOTION SICKNESS HP LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2007-05-29
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
ARNICA MONTANA	30 [hp_C]/mL

OpenFDA Data

• SPL SET ID: 61da7048-b9a9-4af1-b1fc-c30dbaa66f1b
• Manufacturer:
  • Natural Creations, Inc.
• UNII:
  • T7J046YI2B
  • O80TY208ZW
  • QDL83WN8C2
  • BQN1B9B9HA
  • Q28R5GF371
  • KF7Z0E0Q2B
  • QNS6W5US1Z
  • 810258W28U
  • 62I3C8233L
  • 269XH13919
  • 1NM3M2487K
  • 6YR2608RSU
• UPC Code:
  • 0877730002006