NDC 0498-7001

Fem Relief

Acetaminophen Pamabrom

Fem Relief is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Honeywell Safety Products Usa, Inc. The primary component is Acetaminophen; Pamabrom.

Product ID0498-7001_7484e8fa-1396-70e9-e053-2a91aa0a24b7
NDC0498-7001
Product TypeHuman Otc Drug
Proprietary NameFem Relief
Generic NameAcetaminophen Pamabrom
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-01-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameHoneywell Safety Products USA, Inc
Substance NameACETAMINOPHEN; PAMABROM
Active Ingredient Strength325 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 0498-7001-25

250 PACKET in 1 BOX (0498-7001-25) > 2 TABLET in 1 PACKET (0498-7001-01)
Marketing Start Date2017-01-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0498-7001-25 [00498700125]

Fem Relief TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-01-02

NDC 0498-7001-01 [00498700101]

Fem Relief TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-01-01

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN325 mg/1

OpenFDA Data

SPL SET ID:1be326af-0a12-4a69-be5d-32bbffc6dbad
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 313784

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