- SPL UNCLASSIFIED SECTION
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Warnings
Do not use if cap band is missing or broken.
If you are pregnant or nursing, consult a licensed health care professional before using this product.
If symptoms persist for 7 days or worsen, contact a licensed practitioner.
To be used according to label indications and/or standard homeopathic indications
- QUESTIONS
- Directions
- INACTIVE INGREDIENT
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- Principal Display Panel -- 250 Tablet Bottle Label
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INGREDIENTS AND APPEARANCE
NUX VOMICA
nux vomica tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0360-0294 Route of Administration SUBLINGUAL 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] in 1 g Inactive Ingredients Ingredient Name Strength LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) ACACIA (UNII: 5C5403N26O) Product Characteristics Color white Score score with uneven pieces Shape ROUND Size 5mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0360-0294-01 1 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/17/1997 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/17/1997 Labeler - STANDARD HOMEOPATHIC COMPANY (008316655) Establishment Name Address ID/FEI Business Operations STANDARD HOMEOPATHIC COMPANY 008316655 manufacture(0360-0294) , pack(0360-0294) , label(0360-0294)