Label: PHOSPHORUS granule
- NDC Code(s): 62106-5249-4
- 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 October 4, 2023
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ACTIVE INGREDIENT
Active Ingredients
PHOSPHORUS (Phosphorus) 12CH GR
PHOSPHORUS (Phosphorus) 15CH GR
PHOSPHORUS (Phosphorus) 200CH GR
PHOSPHORUS (Phosphorus) 200K GR
PHOSPHORUS (Phosphorus) 30CH GR
PHOSPHORUS (Phosphorus) 30K GR
PHOSPHORUS (Phosphorus) 6CH GR
PHOSPHORUS (Phosphorus) 7CH GR
PHOSPHORUS (Phosphorus) 9CH GR
PHOSPHORUS (Phosphorus) LMK GR
PHOSPHORUS (Phosphorus) MK GR
PHOSPHORUS (Phosphorus) XMK GR
- PURPOSE
- WARNINGS
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- OVERDOSAGE
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- QUESTIONS
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PHOSPHORUS
phosphorus granuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62106-5249 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 4 [hp_X] Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) SUCROSE (UNII: C151H8M554) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62106-5249-4 10 in 1 CARTON 01/29/2015 07/31/2024 1 140 in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/29/2015 07/31/2024 Labeler - Seroyal USA (018361118) Establishment Name Address ID/FEI Business Operations SAN’UP 401010287 manufacture(62106-5249)