Label: CITROMA- magesium citrate liquid
- NDC Code(s): 36800-164-38
- Packager: TOPCO ASSOC, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated July 30, 2024
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- Official Label (Printer Friendly)
- OTHER SAFETY INFORMATION
- Active ingredient (in each fl oz)
- Purpose
- Uses
- Warnings
- Ask a doctor before use if you have
- Ask a doctor or pharmacist before use if you are
- Stop use and ask a doctor if
- if pregnant or breast-feeding
- Keep out of reach of children.
- Other informaiton
-
Directions
- shake well before using
- drink a full glass (8 ounces) of liquid with each dose
- may be taken as a single daily dose or in divided doses
adults and children 12 years of age and over - 6.5 to 10 fl oz in 24 hours
children 6 to under 12 years of age - 3 to 7 fl oz maximum 7 fl oz in 24 hours
children 2 to under 6 years of age - 2 to 3 fl oz in 24 hours
children under 2 years of age - ask a doctor
- other information
- Inactive ingredients
- Questions?
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SPL UNCLASSIFIED SECTION
Non-USP: Non-Carbonated, Non-Pasteurized; CONTAINS PRESERVATIVES
DISTRIBUTED BY TOPCO ASSOC LLC
ELK GROVE VILLAGE, IL 60007
(C)TOPCO VIJA0123
QUESTIONS? 1-888-423-0139
topcare@topco.com www.topcarebrand.com
FORMULA BLENDED IN USA
QUALITY GUARANTEED
This TopCare product is laboratory tested to guarantee its highest quality.
Your total satisfaction is guaranteed.
- principal display panel
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INGREDIENTS AND APPEARANCE
CITROMA
magesium citrate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:36800-164 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MAGNESIUM CITRATE (UNII: RHO26O1T9V) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM CITRATE 1.745 g in 29.6 mL Inactive Ingredients Ingredient Name Strength BENZOIC ACID (UNII: 8SKN0B0MIM) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) SUCRALOSE (UNII: 96K6UQ3ZD4) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36800-164-38 296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/18/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 02/18/2018 Labeler - TOPCO ASSOC, LLC (006935977) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(36800-164)