Label: MUCORSAN- mucor racemosus solution/ drops
- NDC Code(s): 73479-023-04
- Packager: sanPharmacy Inc.
- 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 April 25, 2024
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- Indications
- Dosage
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Warinings
If pregnant or breast-feeding, ask a health professional before use.
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Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.
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When using this product
▪ do not use more than directed
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If symptoms persist more than 5 days, contact a licensed practitioner.
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Tamper Evident: Do not use product if tamper evident strip is broken. To report adverse events, contact MEDsan Inc. at 1-855-462-6334. - Ingredients
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Warnings
If pregnant or breast-feeding, 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 at 1-800-222-1222.
______________________________
When using this product
▪ do not use more than directed
______________________________
If symptoms persist more than 5 days, contact a licensed practitioner.
______________________________
Tamper Evident: Do not use product if tamper evident strip is broken. To report adverse events, contact MEDsan Inc. at 1-855-462-6334. - SPL UNCLASSIFIED SECTION
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INGREDIENTS AND APPEARANCE
MUCORSAN
mucor racemosus solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73479-023 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G) MUCOR RACEMOSUS 4 [hp_X] in 10 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 10 mL in 10 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.09 g in 10 mL POTASSIUM SORBATE (UNII: 1VPU26JZZ4) 0.01 g in 10 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73479-023-04 1 in 1 CARTON 04/25/2024 1 10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/25/2024 Labeler - sanPharmacy Inc. (117235152) Establishment Name Address ID/FEI Business Operations MEDsan Inc. 004326784 manufacture(73479-023)
