Label: MUCORSAN- mucor racemosus suppository
- NDC Code(s): 73479-024-05
- 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 29, 2024
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- Indications
- Dosage
- ACTIVE INGREDIENT
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WARNINGS
If pregnant or breast-feeding, ask a health professional before use.
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Keep out of reach of children. In case of ingestion call Poison Control Center hotline immediately at 1-800-222-1222.
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For rectal use only.
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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: Use this product only if inner blister pack is intact. To report adverse events, contact MEDsan Inc. at 1-855-462-6334. - SPL UNCLASSIFIED SECTION
- Liability statement
- Storage
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MUCORSAN
mucor racemosus suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73479-024 Route of Administration RECTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G) MUCOR RACEMOSUS 3 [hp_X] Inactive Ingredients Ingredient Name Strength HARD FAT (UNII: 8334LX7S21) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73479-024-05 1 in 1 CARTON; Type 0: Not a Combination Product 04/29/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/29/2024 Labeler - sanPharmacy Inc. (117235152) Establishment Name Address ID/FEI Business Operations MEDsan Inc. 004326784 manufacture(73479-024)