Califlora - 53499-5190-4 - (Calendula officinalis)

Alphabetical Index


Drug Information of Califlora

Product NDC: 53499-5190
Proprietary Name: Califlora
Non Proprietary Name: Calendula officinalis
Active Ingredient(s): 1    [hp_X]/78g & nbsp;   Calendula officinalis
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Califlora

Product NDC: 53499-5190
Labeler Name: Nature's Way Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20060101

Package Information of Califlora

Package NDC: 53499-5190-4
Package Description: 1 TUBE in 1 CARTON (53499-5190-4) > 28 g in 1 TUBE

NDC Information of Califlora

NDC Code 53499-5190-4
Proprietary Name Califlora
Package Description 1 TUBE in 1 CARTON (53499-5190-4) > 28 g in 1 TUBE
Product NDC 53499-5190
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Calendula officinalis
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20060101
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Nature's Way Products, Inc.
Substance Name CALENDULA OFFICINALIS FLOWERING TOP
Strength Number 1
Strength Unit [hp_X]/78g
Pharmaceutical Classes

Complete Information of Califlora


General Information