Label: PHOSPHORUS- phosphorus tablet
- NDC Code(s): 54973-2932-4
- Packager: Hyland's
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
COUGH & SORE THROATClose
If you are pregnant or nursing, consult a licensed health care professional before using this product.
Adults: Dissolve 4 tablets under tongue 4 times a day. Children: 2 tablets as above.Close
- INACTIVE INGREDIENT
In a base of Acacia Gum and Lactose N.F.Close
- PRINCIPAL DISPLAY PANEL - 250 Tablet Bottle Label
COUGH & SORE
- INGREDIENTS AND APPEARANCE
Product Information Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:54973-2932 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHOSPHORUS (PHOSPHORUS) PHOSPHORUS 30 [hp_X] Inactive Ingredients Ingredient Name Strength ACACIA LACTOSE Product Characteristics Color YELLOW Score no score Shape ROUND Size 9mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54973-2932-4 250 in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 01/01/1955 Labeler - Hyland's (028570695) Establishment Name Address ID/FEI Business Operations Standard Homeopathic Company 008316655 MANUFACTURE(54973-2932), PACK(54973-2932)