Label: LACTICPLUS- lactic acid, dl- solution/ drops
- NDC Code(s): 59469-024-30
- Packager: PEKANA Naturheilmittel GmbH
- 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 December 21, 2022
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- Indications
- Dosage
- Warning
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 100 ml Bottle Box
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INGREDIENTS AND APPEARANCE
LACTICPLUS
lactic acid, dl- solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59469-024 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Lactic Acid, DL- (UNII: 3B8D35Y7S4) (Lactic Acid, DL- - UNII:3B8D35Y7S4) Lactic Acid, DL- 200 [hp_X] in 100 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:59469-024-30 1 in 1 BOX 04/12/2008 1 100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 04/12/2008 Labeler - PEKANA Naturheilmittel GmbH (320344542) Establishment Name Address ID/FEI Business Operations PEKANA Naturheilmittel GmbH 320344542 MANUFACTURE(59469-024)