NDC 0168-0035

Vitamin A and Vitamin D

Vitamin A And Vitamin D

Vitamin A and Vitamin D is a Topical Ointment in the Human Otc Drug category. It is labeled and distributed by E. Fougera & Co. A Division Of Fougera Pharmaceuticals Inc.. The primary component is Petrolatum.

Product ID0168-0035_3378f795-df7c-4de8-96dd-99afa2f5d4b6
NDC0168-0035
Product TypeHuman Otc Drug
Proprietary NameVitamin A and Vitamin D
Generic NameVitamin A And Vitamin D
Dosage FormOintment
Route of AdministrationTOPICAL
Marketing Start Date1981-01-01
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart347
Labeler NameE. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
Substance NamePETROLATUM
Active Ingredient Strength929 mg/g
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 0168-0035-01

1 TUBE in 1 CARTON (0168-0035-01) > 56.7 g in 1 TUBE
Marketing Start Date1981-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0168-0035-16 [00168003516]

Vitamin A and Vitamin D OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart347
Product TypeHUMAN OTC DRUG
Billing UnitGM
Marketing Start Date1981-01-01
Inactivation Date2020-01-31

NDC 0168-0035-45 [00168003545]

Vitamin A and Vitamin D OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart347
Product TypeHUMAN OTC DRUG
Billing UnitGM
Marketing Start Date2012-09-05
Inactivation Date2020-01-31

NDC 0168-0035-02 [00168003502]

Vitamin A and Vitamin D OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart347
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-09-05
Inactivation Date2020-01-31

NDC 0168-0035-01 [00168003501]

Vitamin A and Vitamin D OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart347
Product TypeHUMAN OTC DRUG
Billing UnitGM
Marketing Start Date1981-01-01
Inactivation Date2020-01-31

NDC 0168-0035-04 [00168003504]

Vitamin A and Vitamin D OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart347
Product TypeHUMAN OTC DRUG
Billing UnitGM
Marketing Start Date2012-09-05
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
PETROLATUM929.3 mg/g

OpenFDA Data

SPL SET ID:b43b9b0d-66d0-4011-b44a-f1fe4adf1ec1
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1303161
  • UPC Code
  • 0301680035161

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