NDC 54973-3324

Baby Nighttime Oral Pain Relief

Arnica Montana, Tribasic Calcium Phosphate, Matricaria Chamomilla, Silicon Dioxide, Magnesium Phosphate, Dibasic Trihydrate, Ferrosoferric Phosphate, Arabica Coffee Bean And Oyster Shell Calcium Carbonate, Crude

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

Product ID54973-3324_71b03f49-4741-2967-e053-2995a90ae089
NDC54973-3324
Product TypeHuman Otc Drug
Proprietary NameBaby Nighttime Oral Pain Relief
Generic NameArnica Montana, Tribasic Calcium Phosphate, Matricaria Chamomilla, Silicon Dioxide, Magnesium Phosphate, Dibasic Trihydrate, Ferrosoferric Phosphate, Arabica Coffee Bean And Oyster Shell Calcium Carbonate, Crude
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-08-17
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHYLAND'S
Substance NameOYSTER SHELL CALCIUM CARBONATE, CRUDE; TRIBASIC CALCIUM PHOSPHATE; MATRICARIA CHAMOMILLA; SILICON DIOXIDE; ARNICA MONTANA; FERROSOFERRIC PHOSPHATE; ARABICA COFFEE BEAN; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
Active Ingredient Strength12 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 54973-3324-1

1 BOTTLE, PLASTIC in 1 CARTON (54973-3324-1) > 1 g in 1 BOTTLE, PLASTIC
Marketing Start Date2017-08-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 54973-3324-1 [54973332401]

Baby Nighttime Oral Pain Relief TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-08-17

NDC 54973-3324-4 [54973332404]

Baby Nighttime Oral Pain Relief TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-08-17

Drug Details

Active Ingredients

IngredientStrength
OYSTER SHELL CALCIUM CARBONATE, CRUDE12 [hp_X]/g

OpenFDA Data

SPL SET ID:58ef86b7-5b38-1591-e053-2991aa0aa53e
Manufacturer
UNII
UPC Code
  • 0354973332416

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