Alumina: Homeopathic Product Information

ALUMINA- aluminum oxide globule
True Botanica, LLC

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.

Alumina 30X, HPUS

The letters HPUS indicate that these ingredients are officially included in the Homeopathic Pharmacopoeia of the United States.


For temporary relief of dry skin/mucous membranes. Helps aging skin. May also be used for standard homeopathic indications or as directed by your physician.


Consult your health care provider if symptoms persist more than 5 days or worsen.

If pregnant or breastfeeding ask a health professional before use.

Keep out of the reach of children.

TAMPER EVIDENT: Do not use if safety seal is broken before first use.

Directions for Use:

Place globules under tongue for 30 seconds. Adults~3-5 globules 3 times a day. Children 2-12 years ~ 1-3
globules 3 times a day. Under 2 years, consult your doctor. Use until symptoms are relieved or as directed by your health care provider.

Other Ingredients:


Developed and Made by

True Botanica, LLC

1005 Richards Rd., Suite D

Hartland, WI 53029


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alumina globule
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:53645-1380
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Inactive Ingredients
Ingredient Name Strength
Product Characteristics
Color white Score no score
Shape ROUND Size 4mm
Flavor Imprint Code
# Item Code Package Description Multilevel Packaging
1 NDC:53645-1380-2 23 g in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 09/02/2013
Labeler — True Botanica, LLC (182071519)
Name Address ID/FEI Operations
True Botanica, LLC 182071519 manufacture (53645-1380)

Revised: 01/2021 True Botanica, LLC provides trustworthy package insert and label information about marketed homeopathic remedies as submitted by manufacturers to the U.S. Food and Drug Administration. Package information is not reviewed or updated separately by Every individual package label entry contains a unique identifier which can be used to secure further details directly from the U.S. National Institutes of Health and/or the FDA.

We source our database directly from the FDA's central repository of homeopathic remedy labels and package inserts, under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

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