NDC directory

ARNICA BRUISE

Arnica montana · Shenzhen Fanyi Era Technology Co., Ltd · CREAM

88028-003UNAPPROVED HOMEOPATHIC
Product NDC
88028-003
Generic name
Arnica montana
Labeler name
Shenzhen Fanyi Era Technology Co., Ltd
Brand name
ARNICA BRUISE
Finished
true
Listing expiration date
20271231
Marketing category
UNAPPROVED HOMEOPATHIC
Dosage form
CREAM
SPL ID
5f47f7cc-d5f5-5037-e063-6394a90a9d2a
Product type
HUMAN OTC DRUG
Marketing start date
20261102
Product ID
88028-003_5f47f7cc-d5f5-5037-e063-6394a90a9d2a
Brand name base
ARNICA BRUISE
Active ingredients
  1. Name
    ARNICA MONTANA
    Strength
    70 mg/g
Packaging
  1. Package NDC
    88028-003-01
    Description
    1 BOTTLE in 1 BOX (88028-003-01) / 113 g in 1 BOTTLE
    Marketing start date
    20261102
    Sample
    false
Route
TOPICAL
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.