Label: NUX VOMICA- strychnos nux-vomica seed pellet
- NDC Code(s): 0220-3681-41, 0220-3681-43
- Packager: Laboratoires Boiron
- Category: HUMAN OTC DRUG LABEL
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 May 22, 2024
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- Official Label (Printer Friendly)
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ACTIVE INGREDIENT
Active ingredient** (in each pellet)
Nux Vomica 30C HPUS
(**contains 0.44 mg of the active ingredient per pellet)(contains less than 10 -12 strychnine alkaloids)
The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.
- PURPOSE
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INDICATIONS & USAGE
Hangover Relief Uses*
temporarily relieves upset stomach associated with nausea or fullness due to overindulgence in drink or food
temporarily relieves occasional heartburn, acid indigestion, or sour stomach
temporarily relieves irritability due to hypersensitivity to light, noise, odor or touch
Indigestion Relief Uses*
temporarily relieves upset stomach associated with nausea or fullness due to overindulgence in drink or food
temporarily relieves occasional heartburn, acid indigestion, or sour stomach
Tube Uses*
Relieves heartburn or drowsiness due to excessive eating or drinking, Irritability *
- WARNINGS
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Hangover Relief
Adults 21 years of age or older: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.
Adults under 21 years of age: Not recommended.
Indigestion Relief
Adults and children 12 years age or older: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.
Children under 12 years of age: Ask a doctor.
Tube
Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.
- INACTIVE INGREDIENT
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SPL UNCLASSIFIED SECTION
Hangover Relief*
On-the-Go Hangover Relief*
No Known Drug Interactions
Upset Stomach Nausea Heartburn Irritability*
do not use if glued carton end flaps are open or if pellet dispenser seal is broken
contains 0.25 g of sugar per dose
retain this carton for full directions
Turn tube upside down. Twist until 5 pellets are dispensed. Remove cap and pour pellets under the tongue.Approx. 80 pellets each
Total 240 pellets
3 Tubes
16 Doses
Indigestion Relief*
Upset or Sour Stomach Heartburn Nausea*
No Known Drug Interactions
do not use if glued carton end flaps are open or if pellet dispenser seal is broken
contains 0.25 g of sugar per dose
retain this carton for full directions
Turn tube upside down. Twist until 5 pellets are dispensed. Remove cap and pour pellets under the tongue.Approx. 80 pellets each
Total 240 pellets
3 Tubes
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
*C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details. - QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NUX VOMICA
strychnos nux-vomica seed pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0220-3681 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 30 [hp_C] Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND (Pellet) Size 4mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0220-3681-43 3 in 1 PACKAGE 01/01/2012 1 NDC:0220-3681-41 80 in 1 TUBE; Type 0: Not a Combination Product 2 NDC:0220-3681-41 80 in 1 TUBE; Type 0: Not a Combination Product 01/01/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/01/2012 Labeler - Laboratoires Boiron (282560473) Registrant - Boiron Inc. (014892269) Establishment Name Address ID/FEI Business Operations Boiron 282560473 manufacture(0220-3681)