A-D-D - 61657-0015-1 - (A-D-D)

Alphabetical Index


Drug Information of A-D-D

Product NDC: 61657-0015
Proprietary Name: A-D-D
Non Proprietary Name: A-D-D
Active Ingredient(s): 10; 10; 10; 10; 10; 10; 10; 10    [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL & nbsp;   A-D-D
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of A-D-D

Product NDC: 61657-0015
Labeler Name: White Manufacturing Incorporated DBA Micro-West
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20110801

Package Information of A-D-D

Package NDC: 61657-0015-1
Package Description: 30 mL in 1 BOTTLE, PUMP (61657-0015-1)

NDC Information of A-D-D

NDC Code 61657-0015-1
Proprietary Name A-D-D
Package Description 30 mL in 1 BOTTLE, PUMP (61657-0015-1)
Product NDC 61657-0015
Product Type Name HUMAN OTC DRUG
Non Proprietary Name A-D-D
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20110801
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name White Manufacturing Incorporated DBA Micro-West
Substance Name BARIUM CARBONATE; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM CARBONATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SODIUM CARBONATE; SODIUM CHLORIDE; STRYCHNOS IGNATII SEED; THUJA OCCIDENTALIS LEAF
Strength Number 10; 10; 10; 10; 10; 10; 10; 10
Strength Unit [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
Pharmaceutical Classes

Complete Information of A-D-D


General Information