Label: MOTION SICKNESS- strychnos nux-vomica seed, tobacco leaf, kerosene, and anamirta cocculus seed tablet, soluble
- NDC Code(s): 54973-9147-1, 54973-9147-2
- Packager: Hyland's Consumer Health 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.
Drug Label Information
Updated September 8, 2022
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- Official Label (Printer Friendly)
- PURPOSE
- Drug Facts
- Uses
- Warnings
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Directions
■ Use as directed.
Adults and children
12 years and overAt onset of symptoms, dissolve 2 tablets under tongue
every 4 hours until relieved, up to 6 times per day.Children 6 years
to under 12 yearsAt onset of symptoms, dissolve 1 tablet under tongue
every 4 hours until relieved, up to 6 times per day. - Inactive Ingredient
- Questions?
- *CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
- DO NOT USE IF TAMPER-EVIDENT SEAL IS BROKEN OR MISSING.
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INGREDIENTS AND APPEARANCE
MOTION SICKNESS
strychnos nux-vomica seed, tobacco leaf, kerosene, and anamirta cocculus seed tablet, solubleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54973-9147 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 6 [hp_X] TOBACCO LEAF (UNII: 6YR2608RSU) (TOBACCO LEAF - UNII:6YR2608RSU) TOBACCO LEAF 6 [hp_X] KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E) KEROSENE 12 [hp_X] ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (ANAMIRTA COCCULUS SEED - UNII:810258W28U) ANAMIRTA COCCULUS SEED 30 [hp_X] Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) Product Characteristics Color white Score no score Shape ROUND Size 9mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54973-9147-1 50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/01/1994 2 NDC:54973-9147-2 1 in 1 CARTON 12/01/1994 2 16 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/01/1994 Labeler - Hyland's Consumer Health Inc. (008316655) Establishment Name Address ID/FEI Business Operations Hyland's Consumer Health Inc. 008316655 manufacture(54973-9147) , pack(54973-9147) , label(54973-9147)