NDC 37000-330

Head and Shoulders Clinical Strength

Selenium Sulfide

Head and Shoulders Clinical Strength is a Topical Lotion/shampoo in the Human Otc Drug category. It is labeled and distributed by The Procter & Gamble Manufacturing Company. The primary component is Selenium Sulfide.

Product ID37000-330_7d62746b-f885-32de-e053-2a91aa0add64
NDC37000-330
Product TypeHuman Otc Drug
Proprietary NameHead and Shoulders Clinical Strength
Generic NameSelenium Sulfide
Dosage FormLotion/shampoo
Route of AdministrationTOPICAL
Marketing Start Date2010-07-01
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart358H
Labeler NameThe Procter & Gamble Manufacturing Company
Substance NameSELENIUM SULFIDE
Active Ingredient Strength1 g/100mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 37000-330-01

2 BOTTLE, PLASTIC in 1 CELLO PACK (37000-330-01) > 400 mL in 1 BOTTLE, PLASTIC
Marketing Start Date2018-11-09
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 37000-330-70 [37000033070]

Head and Shoulders Clinical Strength LOTION/SHAMPOO
Marketing CategoryOTC monograph final
Application Numberpart358H
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-06-13

NDC 37000-330-17 [37000033017]

Head and Shoulders Clinical Strength LOTION/SHAMPOO
Marketing CategoryOTC monograph final
Application Numberpart358H
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-07-01
Marketing End Date2014-09-16

NDC 37000-330-40 [37000033040]

Head and Shoulders Clinical Strength LOTION/SHAMPOO
Marketing CategoryOTC monograph final
Application Numberpart358H
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-07-01

NDC 37000-330-01 [37000033001]

Head and Shoulders Clinical Strength LOTION/SHAMPOO
Marketing CategoryOTC monograph final
Application Numberpart358H
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-11-09

NDC 37000-330-14 [37000033014]

Head and Shoulders Clinical Strength LOTION/SHAMPOO
Marketing CategoryOTC monograph final
Application Numberpart358H
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-07-01
Marketing End Date2014-09-16

Drug Details

Active Ingredients

IngredientStrength
SELENIUM SULFIDE1 g/100mL

OpenFDA Data

SPL SET ID:83cb18cf-627f-4616-92d0-09cbebbc6d1d
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1549328
  • 204642

    • NDC Crossover Matching brand name "Head and Shoulders Clinical Strength" or generic name "Selenium Sulfide"

    NDCBrand NameGeneric Name
    21130-610ANTIDANDRUFFSELENIUM SULFIDE
    0869-0816DandruffSelenium sulfide
    30142-816DandruffSelenium sulfide
    37808-816DandruffSelenium sulfide
    11822-6181Daylogic Maximum Strength DandruffSelenium Sulfide
    37000-330Head and ShouldersSelenium Sulfide
    37808-613HEB DandruffSelenium Sulfide
    30142-519KROGERSELENIUM SULFIDE
    11673-246Medicated DandruffSelenium Sulfide
    30142-246Medicated DandruffSelenium sulfide
    11822-6191RENEWALSELENIUM SULFIDE
    11822-6221RENEWALSELENIUM SULFIDE
    11822-6101Rite AidSELENIUM SULFIDE
    11822-6111Rite Aid Moisturizing DandruffSelenium Sulfide
    11822-6201RITE AID RENEWALSELENIUM SULFIDE
    11822-6211RITE AID RENEWALSELENIUM SULFIDE
    0536-1995Rugby Anti-DandruffSelenium Sulfide
    21130-617SAFEWAYSELENIUM SULFIDE
    21130-620SAFEWAYSELENIUM SULFIDE
    21130-619SAFEWAY CARESELENIUM SULFIDE
    16477-422Selenium SulfideSelenium Sulfide
    16477-423Selenium SulfideSelenium Sulfide
    23710-225TERSIselenium sulfide
    36800-610TopCareSELENIUM SULFIDE
    36800-618TOPCARESELENIUM SULFIDE
    36800-719TOPCARESELENIUM SULFIDE
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