Label: LOA FREEDOM S- sulfate capsule
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Contains inactivated NDC Code(s)
NDC Code(s): 80973-0001-1 - Packager: LOA BIO INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 8, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LOA FREEDOM S
sulfate capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80973-0001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFATE ION (UNII: 7IS9N8KPMG) (SULFATE ION - UNII:7IS9N8KPMG) SULFATE ION 100 g in 100 Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Product Characteristics Color brown Score no score Shape OVAL Size 15mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80973-0001-1 60 in 1 BOTTLE; Type 0: Not a Combination Product 11/09/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/09/2020 Labeler - LOA BIO INC. (695504031) Registrant - LOA BIO INC. (695504031) Establishment Name Address ID/FEI Business Operations LOA BIO INC. 695504031 manufacture(80973-0001)
