NDC 70907-001

Numb Skin

Lidocaine Cream

Numb Skin is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Seenext Venture Ltd. The primary component is Lidocaine.

• Product ID: 70907-001_1034cfed-7374-43a7-9a4a-77bb3104c024
• NDC: 70907-001
• Product Type: Human Otc Drug
• Proprietary Name: Numb Skin
• Generic Name: Lidocaine Cream
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2016-09-01
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part346
• Labeler Name: Seenext Venture Ltd
• Substance Name: LIDOCAINE
• Active Ingredient Strength: 5 mg/30g
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 70907-001-15

1 TUBE in 1 CARTRIDGE (70907-001-15) > 15 g in 1 TUBE

• Marketing Start Date: 2020-04-29
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70907-001-15 [70907000115]

Numb Skin CREAM

• Marketing Category: OTC monograph final
• Application Number: part346
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2020-04-29

NDC 70907-001-30 [70907000130]

Numb Skin CREAM

• Marketing Category: OTC monograph final
• Application Number: part346
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-09-01

Drug Details

Active Ingredients

Ingredient	Strength
LIDOCAINE	5 mg/30g

OpenFDA Data

• SPL SET ID: 3ac18167-774b-3777-e054-00144ff8d46c
• Manufacturer:
  • Seenext Venture Ltd
• UNII:
  • 98PI200987

NDC Crossover Matching brand name "Numb Skin" or generic name "Lidocaine Cream"

NDC	Brand Name	Generic Name
70907-001	Numb Skin	Lidocaine Cream
70907-002	Numb Skin	Lidocaine and Benzethonium Chloride Cream