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- NDC Code(s): 76472-1129-1
- Packager: SEVENE USA
- 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 13, 2023
If you are a consumer or patient please visit this version.
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- ACTIVE INGREDIENT
HOMEOPATHIC DILUTION OF HPUS ARNICA MONTANA 30C
- PURPOSE
TRADITIONALLY USED FOR: PAIN FROM TRAUMA - BRUISES - STIFFNESS - MUSCLE SORENESS.
- DIRECTIONS
(adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.
- USE:
Condition listed above or as directed by a physician.
- WARNINGS
Stop use and ask a physician if symptoms persist for more than 3 days or worsen.
- PREGNANCY OR BREAST FEEDING
If pregnant or breast-feeding, ask a health professional before use.
- KEEP OUT OF REACH OF CHILDREN
Keep out of reach of children.
- OTHER INFORMATION
Store at room temperature.
- DO NOT USE
Do not use if pellet-dispenser seal is broken.
- INACTIVE INGREDIENTS:
Sucrose.
- QUESTIONS?
info@ollois.com
- WWW.OLOIS.COM
- Made in France.
Not reviewed by the FDA and not guaranteed to be effective. This homeopathic dilution may not be susceptible to scientific measurement.
- PRINCIPAL DISPLAY PANEL
- INGREDIENTS AND APPEARANCE
ARNICA 30C
arnica montana pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76472-1129 Route of Administration SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 30[hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score Shape ROUND Size 4mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76472-1129-1 80 in 1 CYLINDER; Type 0: Not a Combination Product 11/30/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/30/2011 Labeler -SEVENE USA(969332936)
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Find additional resources
(also available in the left menu)
Safety
Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk
Related Resources
Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary
More Info on this Drug
View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!
View Labeling Archives for this drug
ARNICA 30C- arnica montana pellet
Number of versions: 17
| Published Date (What is this?) | Version | Files |
|---|---|---|
| Sep 14, 2023 | 26 (current) | download |
| Sep 11, 2023 | 25 | download |
| Jun 9, 2021 | 24 | download |
| Jun 7, 2021 | 23 | download |
| Jun 3, 2021 | 22 | download |
| Mar 18, 2020 | 21 | download |
| Apr 22, 2019 | 20 | download |
| May 3, 2018 | 18 | download |
| Apr 26, 2018 | 17 | download |
| May 18, 2017 | 12 | download |
| Mar 22, 2017 | 10 | download |
| Jul 11, 2016 | 8 | download |
| Jan 6, 2016 | 6 | download |
| Jan 4, 2016 | 5 | download |
| Dec 29, 2015 | 4 | download |
| Dec 2, 2013 | 3 | download |
| Dec 1, 2011 | 1 | download |
RxNorm
ARNICA 30C- arnica montana pellet
Under Review - Editing is pending for RxNorm. If in scope, these drugs will include RxNorm normal forms when editing is complete.
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ARNICA 30C- arnica montana pellet
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NDC Codes
ARNICA 30C- arnica montana pellet
If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such.
| NDC | |
|---|---|
| 1 | 76472-1129-1 |
