NDC 54973-3245

4Kids Cold n Cough Nighttime Grape Flavor

Onion, Matricaria Recutita, Arabica Coffee Bean, Calcium Sulfide, Goldenseal, Sodium Chloride, Strychnos Nux-vomica Seed, Phosphorus, Anemone Pulsatilla, And Sulfur

4Kids Cold n Cough Nighttime Grape Flavor is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Hyland's. The primary component is Onion; Matricaria Recutita; Arabica Coffee Bean; Calcium Sulfide; Goldenseal; Sodium Chloride; Strychnos Nux-vomica Seed; Phosphorus; Anemone Pulsatilla; Sulfur.

• Product ID: 54973-3245_5fb346ae-a31c-2099-e053-2a91aa0acb93
• NDC: 54973-3245
• Product Type: Human Otc Drug
• Proprietary Name: 4Kids Cold n Cough Nighttime Grape Flavor
• Generic Name: Onion, Matricaria Recutita, Arabica Coffee Bean, Calcium Sulfide, Goldenseal, Sodium Chloride, Strychnos Nux-vomica Seed, Phosphorus, Anemone Pulsatilla, And Sulfur
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2016-04-18
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Hyland's
• Substance Name: ONION; MATRICARIA RECUTITA; ARABICA COFFEE BEAN; CALCIUM SULFIDE; GOLDENSEAL; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; PHOSPHORUS; ANEMONE PULSATILLA; SULFUR
• Active Ingredient Strength: 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 54973-3245-1

1 BOTTLE, PLASTIC in 1 CARTON (54973-3245-1) > 118 mL in 1 BOTTLE, PLASTIC

• Marketing Start Date: 2016-04-18
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 54973-3245-2 [54973324502]

4Kids Cold n Cough Nighttime Grape Flavor LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-04-18
• Marketing End Date: 2020-01-01

NDC 54973-3245-1 [54973324501]

4Kids Cold n Cough Nighttime Grape Flavor LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-04-18
• Marketing End Date: 2020-01-01

Drug Details

Active Ingredients

Ingredient	Strength
ONION	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 42b4f577-2654-4e67-8387-0191ef8aa0e4
• Manufacturer:
  • Hyland's
• UNII:
  • ZW3Z11D0JV
  • 70FD1KFU70
  • 451W47IQ8X
  • 492225Q21H
  • I76KB35JEV
  • 27YLU75U4W
  • G0R4UBI2ZZ
  • 269XH13919
  • 1MBW07J51Q
  • 3SW678MX72