NDC 81902-201

Zylotrol

Lidocaine Hcl 4%, Menthol 1%

Zylotrol is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Whitestone Products Llc. The primary component is Lidocaine Hydrochloride; Menthol, Unspecified Form.

• Product ID: 81902-201_d4cec57f-6660-793c-e053-2a95a90a995c
• NDC: 81902-201
• Product Type: Human Otc Drug
• Proprietary Name: Zylotrol
• Generic Name: Lidocaine Hcl 4%, Menthol 1%
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2022-01-04
• Marketing Category: OTC MONOGRAPH NOT FINAL /
• Application Number: part348
• Labeler Name: Whitestone Products LLC
• Substance Name: LIDOCAINE HYDROCHLORIDE; MENTHOL, UNSPECIFIED FORM
• Active Ingredient Strength: 4 g/100g; g/100g
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 81902-201-04

1 TUBE in 1 BOX (81902-201-04) > 118.3 g in 1 TUBE

• Marketing Start Date: 2022-01-04
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Zylotrol" or generic name "Lidocaine Hcl 4%, Menthol 1%"

NDC	Brand Name	Generic Name
76420-145	Zylotrol	Lidocaine HCl 4%, Menthol 1%
76420-504	Zylotrol	Lidocaine 4%, Menthol 4%
81902-130	Zylotrol	Lidocaine 4%, Menthol 4%
81902-201	Zylotrol	Lidocaine HCl 4%, Menthol 1%