NDC 70796-003

Puriton FACIAL SKIN PROTECTANT AND ACNE TREATMENT HOMEOPATHIC

Alumina, Calcarea Silicata, Ferrum Metallicum, Magnesia Sulphurica, Phosphorous, Sulphur, Titanium Metallicum, Zincum Metallicum

Puriton FACIAL SKIN PROTECTANT AND ACNE TREATMENT HOMEOPATHIC is a Topical Solution in the Human Otc Drug category. It is labeled and distributed by Kadesh, Inc.. The primary component is Aluminum Oxide; Calcium Silicate; Iron; Magnesium Sulfate Heptahydrate; Phosphorus; Sulfur; Titanium; Zinc.

Product ID70796-003_d2f1e75f-0a90-49c4-8450-e8d8f0cbab97
NDC70796-003
Product TypeHuman Otc Drug
Proprietary NamePuriton FACIAL SKIN PROTECTANT AND ACNE TREATMENT HOMEOPATHIC
Generic NameAlumina, Calcarea Silicata, Ferrum Metallicum, Magnesia Sulphurica, Phosphorous, Sulphur, Titanium Metallicum, Zincum Metallicum
Dosage FormSolution
Route of AdministrationTOPICAL
Marketing Start Date2016-10-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameKadesh, Inc.
Substance NameALUMINUM OXIDE; CALCIUM SILICATE; IRON; MAGNESIUM SULFATE HEPTAHYDRATE; PHOSPHORUS; SULFUR; TITANIUM; ZINC
Active Ingredient Strength7 [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 70796-003-04

1 BOTTLE in 1 CARTON (70796-003-04) > 118 mL in 1 BOTTLE
Marketing Start Date2016-10-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70796-003-04 [70796000304]

Puriton FACIAL SKIN PROTECTANT AND ACNE TREATMENT HOMEOPATHIC SOLUTION
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ALUMINUM OXIDE7 [hp_X]/118mL

OpenFDA Data

SPL SET ID:be28e865-a21e-4554-80d7-704d33f2b2e4
Manufacturer
UNII
UPC Code
  • 0736972167983

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