NDC 64269-9903

Scarguard MD

Hydrocortisone Silicone

Scarguard MD is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Scarguard Labs, Llc. The primary component is Hydrocortisone; Phenyl Trimethicone.

• Product ID: 64269-9903_617c546b-3088-405c-bc14-d1759573976e
• NDC: 64269-9903
• Product Type: Human Otc Drug
• Proprietary Name: Scarguard MD
• Generic Name: Hydrocortisone Silicone
• Dosage Form: Liquid
• Route of Administration: TOPICAL
• Marketing Start Date: 2001-11-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part348
• Labeler Name: Scarguard Labs, LLC
• Substance Name: HYDROCORTISONE; PHENYL TRIMETHICONE
• Active Ingredient Strength: 5 mg/mL; mL/100mL
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 64269-9903-8

30 mL in 1 BOTTLE, WITH APPLICATOR (64269-9903-8)

• Marketing Start Date: 2001-11-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 64269-9903-7 [64269990307]

Scarguard MD LIQUID

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2001-11-01
• Inactivation Date: 2020-01-31

NDC 64269-9903-8 [64269990308]

Scarguard MD LIQUID

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2001-11-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
HYDROCORTISONE	5 mg/mL

OpenFDA Data

• SPL SET ID: eef21e54-c5fc-48ab-a514-97ba805ffea8
• Manufacturer:
  • Scarguard Labs, LLC
• UNII:
  • DR0K5NOJ4R
  • WI4X0X7BPJ
• UPC Code:
  • 0364269101008

NDC Crossover Matching brand name "Scarguard MD" or generic name "Hydrocortisone Silicone"

NDC	Brand Name	Generic Name
64269-9903	Scarguard MD	Hydrocortisone Silicone
64269-9909	Scarguard MD Physicians Formula	Hydrocortisone Silicone