NUX VOMICA: Homeopathic Product Information

NUX VOMICA- strychnos nux-vomica seed tablet
Hyland’s Inc.

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.

NUX VOMICA 30X

NAUSEA, HEADACHE OR FLU

NAUSEA, HEADACHE OR FLU

Made according to the Homeopathic Pharmacopoeia of the United States since 1903.

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.

Keep this and all medicines out of the reach of children.

To be used according to label indications and/or standard homeopathic indications.

Directions

Adults: Dissolve 4 tablets under tongue 4 times a day.

Children: consult a healthcare professional.

Inactive Ingredients

Acacia Gum and Lactose

Questions?

800-624-9659

PRINCIPAL DISPLAY PANEL — 250 Tablet Bottle Label

SINCE 1903
Hyland’s ®
HOMEOPATHIC

NDC 54973-2921-4

NUX VOMICA

30X

NAUSEA, HEADACHE OR

FLU *

250 TABLETS

*Claims are based on traditional

homeopathic practice, not

accepted medical evidence.

Not FDA evaluated.

Label
(click image for full-size original)
NUX VOMICA
strychnos nux-vomica seed tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:54973-2921
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
STRYCHNOS NUX-VOMICA SEED (STRYCHNOS NUX-VOMICA SEED) STRYCHNOS NUX-VOMICA SEED 30 [hp_X]
Inactive Ingredients
Ingredient Name Strength
ACACIA
LACTOSE
Product Characteristics
Color brown Score no score
Shape ROUND Size 9mm
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:54973-2921-4 250 TABLET in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 01/01/1955
Labeler — Hyland’s Inc. (008316655)
Establishment
Name Address ID/FEI Operations
Hyland’s Inc. 008316655 manufacture (54973-2921), pack (54973-2921)

Revised: 12/2022 Hyland’s Inc.

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