NDC 50154-012

All Day Skin Relief with Colloidal Oats

Cetyl Alcohol

All Day Skin Relief with Colloidal Oats is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Lantern Enterprises Ltd.. The primary component is Cetyl Alcohol.

• Product ID: 50154-012_32c041a6-afee-461b-e054-00144ff88e88
• NDC: 50154-012
• Product Type: Human Otc Drug
• Proprietary Name: All Day Skin Relief with Colloidal Oats
• Generic Name: Cetyl Alcohol
• Dosage Form: Lotion
• Route of Administration: TOPICAL
• Marketing Start Date: 2016-05-13
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Lantern Enterprises Ltd.
• Substance Name: CETYL ALCOHOL
• Active Ingredient Strength: 80 mg/100mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 50154-012-50

354 mL in 1 BOTTLE (50154-012-50)

• Marketing Start Date: 2016-05-13
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 50154-012-50 [50154001250]

All Day Skin Relief with Colloidal Oats LOTION

• Marketing Category: unapproved drug other
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-05-13
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
CETYL ALCOHOL	80 mg/100mL

OpenFDA Data

• SPL SET ID: 31e07369-e63e-439c-e054-00144ff88e88
• Manufacturer:
  • Lantern Enterprises Ltd.
• UNII:
  • 936JST6JCN

NDC Crossover Matching brand name "All Day Skin Relief with Colloidal Oats" or generic name "Cetyl Alcohol"

NDC	Brand Name	Generic Name
50154-012	All Day Skin Relief with Colloidal Oats	CETYL ALCOHOL
50306-011	All Day Skin Relief with Colloidal Oats	CETYL ALCOHOL