Label: PLEO FORM- formic acid solution/ drops
Contains inactivated NDC Code(s)
NDC Code(s): 60681-0114-3
- Packager: Sanum Kehlbeck GmbH & Co. KG
- 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 May 23, 2012
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- ACTIVE INGREDIENT
- Tamper Evident
As with any drug, if you are pregnant or nursing a baby, seek the advice of health care professional before using this product.
- STORAGE AND HANDLING
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton
INGREDIENTS AND APPEARANCE
formic acid solution/ drops
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60681-0114 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength formic acid (UNII: 0YIW783RG1) (formic acid - UNII:0YIW783RG1) formic acid 200 [hp_X] in 30 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) alcohol (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60681-0114-3 1 in 1 CARTON 1 30 mL in 1 BOTTLE, DROPPER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved homeopathic 12/09/2004 Labeler - Sanum Kehlbeck GmbH & Co. KG (318386133)