NDC 60512-9077

ALLERGY KIDS RELIEF

Pulsatilla, Allium Cepa, Arsenicum Album, Nux Vomica, Euphrasia Officinalis, Sabadilla, Sticta Pulmonaria, Aralia Racemosa, Cuprum Metallicum

ALLERGY KIDS RELIEF is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc. The primary component is Pulsatilla Vulgaris; Onion; Arsenic Trioxide; Strychnos Nux-vomica Seed; Euphrasia Stricta; Schoenocaulon Officinale Seed; Lobaria Pulmonaria; Aralia Racemosa Root; Copper.

Product ID60512-9077_a02a5db7-ffe3-4c8f-8bf2-0b146856e42a
NDC60512-9077
Product TypeHuman Otc Drug
Proprietary NameALLERGY KIDS RELIEF
Generic NamePulsatilla, Allium Cepa, Arsenicum Album, Nux Vomica, Euphrasia Officinalis, Sabadilla, Sticta Pulmonaria, Aralia Racemosa, Cuprum Metallicum
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2009-04-20
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHOMEOLAB USA INC
Substance NamePULSATILLA VULGARIS; ONION; ARSENIC TRIOXIDE; STRYCHNOS NUX-VOMICA SEED; EUPHRASIA STRICTA; SCHOENOCAULON OFFICINALE SEED; LOBARIA PULMONARIA; ARALIA RACEMOSA ROOT; COPPER
Active Ingredient Strength8 [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 60512-9077-8

1 BOTTLE in 1 CARTON (60512-9077-8) > 25 mL in 1 BOTTLE
Marketing Start Date2009-04-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 60512-9077-8 [60512907708]

ALLERGY KIDS RELIEF LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-04-20
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
PULSATILLA VULGARIS8 [hp_X]/25mL

OpenFDA Data

SPL SET ID:b9f9b8cc-2154-4a84-ad8e-3324b16ffc77
Manufacturer
UNII
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