Label: TOTAL ALUMINUM- aluminum metal liquid
- NDC Code(s): 61657-0955-1
- Packager: White Manufacturing Inc. DBA Micro-West
- Category: HUMAN OTC DRUG LABEL
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 January 21, 2021
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- Directions
- INDICATIONS
- Active Ingredients
- WARNING
- OTHER SAFETY INFORMATION
- Keep out of reach of children
- Inactive Ingredient
- Purpose
- Label
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INGREDIENTS AND APPEARANCE
TOTAL ALUMINUM
aluminum metal liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61657-0955 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM (UNII: CPD4NFA903) (ALUMINUM - UNII:CPD4NFA903) ALUMINUM 12 [hp_X] in 30 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61657-0955-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 09/30/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/30/2011 Labeler - White Manufacturing Inc. DBA Micro-West (082307831)