Bikini Zone Medicated Gel

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Bikini Zone Medicated Gel
Generic name
LIDOCAINE
Manufacturer
Kingsway Pharmaceuticals dba NFI, LLC
Product type
HUMAN OTC DRUG
SPL set ID
30b85890-e72d-4af7-bda9-e7744abc92af
SPL ID
30b85890-e72d-4af7-bda9-e7744abc92af
Version
1
Effective date
2025-08-29
Source export date
2026-08-01
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/4d7120b2932458966cd5c2f0e3ab49319f616f09498d059c9ff283a8dac64565/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:11:30
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Avoid contact with eyes Do not use in large quantities, particularly over raw surfaces or blistered areas Stop use and ask a doctor if • Condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Discontinue use. Keep out of reach of children • If product is swallowed, get medical help or contact a Poison Control Center right away.