NDC 54973-3391

Baby Oral Pain Relief Drops

Ferrosoferric Phosphate,tribasic Calcium Phosphate,oyster Shell Calcium Carbonate,crude,arnica Montana,arabica Coffee Bean And Matricaria Chamomilla

Baby Oral Pain Relief Drops is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Hyland's. The primary component is Arnica Montana; Oyster Shell Calcium Carbonate, Crude; Tribasic Calcium Phosphate; Ferrosoferric Phosphate; Arabica Coffee Bean; Matricaria Chamomilla.

Product ID54973-3391_7ffe2d76-254b-1406-e053-2991aa0afb61
NDC54973-3391
Product TypeHuman Otc Drug
Proprietary NameBaby Oral Pain Relief Drops
Generic NameFerrosoferric Phosphate,tribasic Calcium Phosphate,oyster Shell Calcium Carbonate,crude,arnica Montana,arabica Coffee Bean And Matricaria Chamomilla
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2019-01-24
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHyland's
Substance NameARNICA MONTANA; OYSTER SHELL CALCIUM CARBONATE, CRUDE; TRIBASIC CALCIUM PHOSPHATE; FERROSOFERRIC PHOSPHATE; ARABICA COFFEE BEAN; MATRICARIA CHAMOMILLA
Active Ingredient Strength30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 54973-3391-1

1 BOTTLE, PLASTIC in 1 CARTON (54973-3391-1) > 29.6 mL in 1 BOTTLE, PLASTIC
Marketing Start Date2019-01-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 54973-3391-1 [54973339101]

Baby Oral Pain Relief Drops LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-24

Drug Details

Active Ingredients

IngredientStrength
ARNICA MONTANA30 [hp_X]/mL

OpenFDA Data

SPL SET ID:7ffe2d76-254a-1406-e053-2991aa0afb61
Manufacturer
UNII
UPC Code
  • 0354973339118
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