Label: LETOMINT- clove tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 76255-2001-1 - Packager: H&C 21 America Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated June 18, 2011
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
- women that the lower abdoment or the hands and feet are cold
- women who have period pain and menstrual irregularity or have a light or heavy flow during your period
- women that have serious vaginal discharge
- women who try to prevent urinary incontinence
- women who feel that their vaginal muscle is relaxed after delivery
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LETOMINT
clove tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76255-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLOVE (UNII: K48IKT5321) (CLOVE - UNII:K48IKT5321) CLOVE 18 mg Inactive Ingredients Ingredient Name Strength ALUMINUM SULFATE (UNII: 34S289N54E) GARLIC (UNII: V1V998DC17) POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE (UNII: V5VD430YW9) WATER (UNII: 059QF0KO0R) Product Characteristics Color white (ivory white) Score no score Shape OVAL (tablet) Size 10mm Flavor Imprint Code 3;hp;x Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76255-2001-1 18 in 1 BOX Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/18/2011 Labeler - H&C 21 America Inc (968313267) Registrant - H&C 21 America Inc (968313267) Establishment Name Address ID/FEI Business Operations GM Manufacturing Inc 102301749 manufacture