Label: MUCO COCCINUM- klebsiella pneumoniae tablet
- NDC Code(s): 62106-6870-0
- Packager: Seroyal USA
- 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 November 9, 2022
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
-
WARNINGS
Warnings
This product is not intended to be an alternative to
vaccination.
Do not use if you have ever had an allergic reaction to this
product or any of its ingredients.
Stop use and ask a doctor if symptoms continue to persist
after three days of use or are accompanied by a fever.
If pregnant or breastfeeding, ask a health professional before
use. Keep out of reach of children. In case of overdose, get
medical help or contact a Poison Control Center right away. - DO NOT USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- OVERDOSAGE
- INACTIVE INGREDIENT
- OTHER SAFETY INFORMATION
-
DOSAGE & ADMINISTRATION
Directions
Adults and Adolescents (12 years and older): At the first sign of symptoms, take one tablet allowing it to dissolve under the tongue. If
symptoms persist, take one tablet two or three times during the day or as recommended by your healthcare practitioner.Children (6-11 years): Take under the direction of your healthcare practitioner.
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INDICATIONS & USAGE
Uses
For the temporary relief of cold and flu-like symptoms.
Directions
Adults and Adolescents (12 years and older): At the first sign of symptoms, take one tablet allowing it to dissolve under the tongue. If
symptoms persist, take one tablet two or three times during the day or as recommended by your healthcare practitioner.Children (6-11 years): Take under the direction of your healthcare practitioner.
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MUCO COCCINUM
klebsiella pneumoniae tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62106-6870 Route of Administration SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANAEROCOCCUS TETRADIUS (UNII: 7Q9DHH4FGG) (ANAEROCOCCUS TETRADIUS - UNII:7Q9DHH4FGG) ANAEROCOCCUS TETRADIUS 200 [hp_C] INFLUENZA A VIRUS (UNII: R9HH0NDE2E) (INFLUENZA A VIRUS - UNII:R9HH0NDE2E) INFLUENZA A VIRUS 200 [hp_C] INFLUENZA B VIRUS (UNII: 1314JZ2X6W) (INFLUENZA B VIRUS - UNII:1314JZ2X6W) INFLUENZA B VIRUS 200 [hp_C] KLEBSIELLA PNEUMONIAE (UNII: 09PA36CT5R) (KLEBSIELLA PNEUMONIAE - UNII:09PA36CT5R) KLEBSIELLA PNEUMONIAE 200 [hp_C] MORAXELLA CATARRHALIS SUBSP. CATARRHALIS (UNII: 1X259JGO78) (MORAXELLA CATARRHALIS SUBSP. CATARRHALIS - UNII:1X259JGO78) MORAXELLA CATARRHALIS SUBSP. CATARRHALIS 200 [hp_C] Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) LACTOSE (UNII: J2B2A4N98G) MAGNESIUM STEARATE (UNII: 70097M6I30) XYLITOL (UNII: VCQ006KQ1E) Product Characteristics Color white Score no score Shape ROUND Size 9mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62106-6870-0 1 in 1 BOX 10/15/2014 1 10 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/15/2014 Labeler - Seroyal USA (018361118) Establishment Name Address ID/FEI Business Operations SAN’UP 401010287 manufacture(62106-6870)
NDC 62106-6870-0