NDC 67777-232

Lanolin

Lanolin

Lanolin is a Topical Ointment in the Human Otc Drug category. It is labeled and distributed by Dynarex Corporation. The primary component is Lanolin.

Product ID67777-232_a2902a28-599d-4c10-8a0c-957b4bed94f2
NDC67777-232
Product TypeHuman Otc Drug
Proprietary NameLanolin
Generic NameLanolin
Dosage FormOintment
Route of AdministrationTOPICAL
Marketing Start Date2010-05-12
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart347
Labeler NameDynarex Corporation
Substance NameLANOLIN
Active Ingredient Strength50 g/100g
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 67777-232-04

24 TUBE in 1 CASE (67777-232-04) > 113 g in 1 TUBE
Marketing Start Date2010-05-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67777-232-03 [67777023203]

Lanolin OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart347
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-05-12
Inactivation Date2020-01-31

NDC 67777-232-06 [67777023206]

Lanolin OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart347
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-05-12
Inactivation Date2020-01-31

NDC 67777-232-01 [67777023201]

Lanolin OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart347
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-05-12
Inactivation Date2020-01-31

NDC 67777-232-02 [67777023202]

Lanolin OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart347
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-05-12
Inactivation Date2020-01-31

NDC 67777-232-04 [67777023204]

Lanolin OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart347
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-05-12
Inactivation Date2020-01-31

NDC 67777-232-05 [67777023205]

Lanolin OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart347
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-05-12
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
LANOLIN50 g/100g

OpenFDA Data

SPL SET ID:87216888-1753-4fd5-a8e0-d8347948b082
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 853167
  • UPC Code
  • 0616784126319
  • NDC Crossover Matching brand name "Lanolin" or generic name "Lanolin"

    NDCBrand NameGeneric Name
    67777-232LanolinLanolin
    68786-232LanolinLanolin
    60764-1113CE DRAWING LIP CHILLINGLanolin
    71289-1014sport skincare anti chafingLanolin
    52410-8050AmeriDermLanolin
    11822-3271Baby Care Vitamins A and DLanolin
    82806-001Black RoseLANOLIN
    61767-232Lana1263Lanolin
    67777-410LanashieldLanolin
    12090-0042LanoGuardLANOLIN
    12090-0074LanoGuardLANOLIN
    61924-504Lantiseptic by Dermarite Dry Skin TherapyLANOLIN
    61924-304Lantiseptic by DermaRite Original Skin ProtectantLANOLIN
    12090-0016Lantiseptic Dry Skin TherapyLANOLIN
    61924-710Lantiseptic Dry Skin TherapyLANOLIN
    12090-0019Lantiseptic Original Skin ProtectantLANOLIN
    69636-8050LincoFixLanolin
    75904-3343PrimaGuardLANOLIN
    68345-818ReparaLanolin
    68599-6202Skin Protectant with LanolinLanolin
    68599-6203Skin Protectant with LanolinLanolin
    70196-1333Smartchoices Lanolin PlusLanolin
    53329-042Soothe and Cool Free MedsepticLanolin
    72184-001Theresienol MD Skin ProtectantLanolin
    11527-325Theriac Advanced HealingLanolin

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.