NDC 59262-502

BABY GUM RELIEF

Calcium Fluoride, Chamomile, Ferrum Phosphoricum, Oyster Shell Calcium Carbonate, Crude, Podophyllum And Tribasic Calcium Phosphate

BABY GUM RELIEF is a Oral Tablet, Orally Disintegrating in the Human Otc Drug category. It is labeled and distributed by Similasan Corporation. The primary component is Oyster Shell Calcium Carbonate, Crude; Calcium Fluoride; Tribasic Calcium Phosphate; Chamomile; Ferrosoferric Phosphate; Podophyllum.

Product ID59262-502_b0b8413d-2d5b-4e27-a213-5573dd1e3e0d
NDC59262-502
Product TypeHuman Otc Drug
Proprietary NameBABY GUM RELIEF
Generic NameCalcium Fluoride, Chamomile, Ferrum Phosphoricum, Oyster Shell Calcium Carbonate, Crude, Podophyllum And Tribasic Calcium Phosphate
Dosage FormTablet, Orally Disintegrating
Route of AdministrationORAL
Marketing Start Date2018-06-15
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameSimilasan Corporation
Substance NameOYSTER SHELL CALCIUM CARBONATE, CRUDE; CALCIUM FLUORIDE; TRIBASIC CALCIUM PHOSPHATE; CHAMOMILE; FERROSOFERRIC PHOSPHATE; PODOPHYLLUM
Active Ingredient Strength12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 59262-502-26

1 BOTTLE in 1 BOX (59262-502-26) > 135 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE
Marketing Start Date2018-06-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 59262-502-26 [59262050226]

BABY GUM RELIEF TABLET, ORALLY DISINTEGRATING
Marketing CategoryUNAPPROVED HOMEOPATHIC
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-06-15
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
OYSTER SHELL CALCIUM CARBONATE, CRUDE12 [hp_X]/1

OpenFDA Data

SPL SET ID:5d49e61d-7bd1-4211-bbad-80da9d7dfabf
Manufacturer
UNII
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.