NDC 68229-201-09 - Alocane Emergency Burn

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
68229-201
Requested NDC
68229-201-09
Package NDCs from labels
68229-201-01, 68229-201-02, 68229-201-03, 68229-201-04, 68229-201-05, 68229-201-06, 68229-201-07, 68229-201-08, 68229-201-11, 68229-201-09, 68229-201-10, 68229-201-14, 68229-201-15, 68229-201-12, 68229-201-13, 68229-201-17, 68229-201-18, 68229-201-16
Manufacturer
Quest Products, LLC. | Fill Tech USA
Effective date
2026-10-22
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Alocane Emergency Burn - Quest Products, LLC. | Fill Tech USAQuest Products, LLC. | Fill Tech USA2026-10-22HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68229-201-01Alocane Emergency Burn110 mL in 1 TUBEGEL11014
68229-201-02Alocane Emergency Burn1 in 1 CARTONGEL114
68229-201-03Alocane Emergency Burn110 mL in 1 BOTTLE, SPRAYGEL11014
68229-201-04Alocane Emergency Burn3.4 mL in 1 PACKETGEL3.414
68229-201-05Alocane Emergency Burn24 in 1 CARTONGEL2414
68229-201-06Alocane Emergency Burn3.4 mL in 1 PACKETGEL3.414
68229-201-07Alocane Emergency Burn45 in 1 CARTONGEL4514
68229-201-08Alocane Emergency Burn103.507 mL in 1 BOTTLE, SPRAYGEL103.50714
68229-201-09Alocane Emergency Burn118.294 mL in 1 TUBEGEL118.29414
68229-201-10Alocane Emergency Burn1 in 1 CARTONGEL114
68229-201-11Alocane Emergency Burn133.081 mL in 1 BOTTLE, SPRAYGEL133.08114
68229-201-12Alocane Emergency Burn1 in 1 KITGEL114
68229-201-13Alocane Emergency Burn1 in 1 CARTONGEL114
68229-201-14Alocane Emergency Burn946 mL in 1 BOTTLE, PUMPGEL94614
68229-201-15Alocane Emergency Burn800 mL in 1 BAGGEL80014
68229-201-16Alocane Emergency Burn124 mL in 1 BOTTLE, SPRAYGEL12414
68229-201-17Alocane Emergency Burn22 mL in 1 TUBEGEL2214
68229-201-18Alocane Emergency Burn1 in 1 CARTONGEL114

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68229-201ALOCANE EMERGENCY BURN (LIDOCAINE HYDROCHLORIDE) GEL [QUEST PRODUCTS, LLC.]14Legacy NDC, 18 package rows20241107_0c8e65a6-dff3-43b4-a3f1-95deb574ea89.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 42 · 823 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LIDOCAINE HYDROCHLORIDELIDOCAINE HYDROCHLORIDEHenry Schein, Inc.23c8f711-e458-479a-9ab0-dcc851311e242026-09-10Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Burn CreamBENZALKONIUM CHLORIDE, LIDOCAINE HCITrifecta Pharmaceuticals USA LLCe9a9fc7c-31da-ea3f-e053-2a95a90a0eab2026-09-09WarningsExact identifier
unii: V13007Z41A
Burn GelLIDOCAINE HCITrifecta Pharmaceuticals USA LLCe9d3e9be-1036-fad0-e053-2a95a90a6efe2026-09-09WarningsExact identifier
unii: V13007Z41A
American Safety First AidLIDOCAINE HCLOrazen Incea2f776b-dfd0-6ce4-e053-2995a90af0092026-09-07WarningsExact identifier
unii: V13007Z41A
MEDI-FIRST Topical AnalgesicLIDOCAINE HCIUltra Distributors Incb6f288f7-9ae3-215e-e053-2a95a90aedf62026-09-07WarningsExact identifier
unii: V13007Z41A
MEDI-FIRSTBENZALKONIUM CHLORIDE, LIDOCAINEOrazen Incf508434f-5948-7134-e053-2a95a90a03d72026-09-05WarningsExact identifier
unii: V13007Z41A
MEDI-FIRSTBENZALKONIUM CHLORIDE, LIDOCAINEOrazen Incf522fb0b-3d86-b228-e053-2a95a90a55e92026-09-05WarningsExact identifier
unii: V13007Z41A
Nerve Guard Nerve ReliefLIDOCAINE HYDROCHLORIDE, MENTHOL,MAGNESIUM CHLORIDEMicelle Laboratories, Incorporated6b78f40f-2a7f-4c49-96af-1a95acbf430f2026-09-04WarningsExact identifier
unii: V13007Z41A
Lidocaine ViscousLIDOCAINE HYDROCHLORIDEREMEDYREPACK INC.6f8d20d2-6a91-4a5b-bfe8-f1baada384422026-09-03Boxed warning, Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
HUSTLE BUTTER NUMBINGLIDOCAINE HCL, BENZALKONIUM CHLORIDEH.B.D. DIST. INC.5b4d0390-dac6-4a71-9fdc-5c31543e7c5a2026-09-02WarningsExact identifier
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEPAI Holdings, LLC dba PAI Pharma9920daef-b156-4a14-b641-f714191ffb5c2026-09-02Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEREMEDYREPACK INC.f824b48c-7039-4ce1-b3df-b3597aba5beb2026-08-28Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
KUGIG ALOE FOAMING INTIMATE WASHINTIMATE CLEANSING FOAMHong Kong KangXing Centennial Management Limited59f4d398-1186-a168-e063-6294a90ab44b2026-08-26WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERREMEDYREPACK INC.5dd5d148-6e23-41de-bff5-551b2aea95982026-08-24Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
HUSTLE BUTTER NUMBINGLIDOCAINE HYDROCHLORIDEH.B.D. D.I.S.T. INC.d7dfb312-6c80-4a2d-b8b2-d9891cb0b74e2026-08-24WarningsExact identifier
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEHospira, Inc.ad1ef0a8-88db-4648-c098-d009eaeb4e5b2026-08-20Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEMajor Pharmaceuticals04e8dd94-93a8-427d-81ab-a95793d86c362026-08-18Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
BM BM63 DROPSCEANOTHUS, KALI ARSEN, KALI MUR, SELENIUM, THALLIUM, WIESBADENBM Private Limited59006d82-610a-2e08-e063-6394a90af1ed2026-08-14WarningsExact identifier
unii: 059QF0KO0R
JJ Care First Aid BurnBENZALKONIUM CHLORIDE, LIDOCAINE HCINantong Health & Beyond Hygienic Products Inc.c41621fb-c549-4394-a4cb-cb81ef8c98df2026-08-13WarningsExact identifier
unii: V13007Z41A
XylocaineLIDOCAINE HYDROCHLORIDE AND EPINEPHRINE BITARTRATEDentsply Pharmaceutical14b55cf9-f7cd-4bb4-a7c5-aba61abadef12026-08-13Warnings, Adverse reactionsExact identifier
unii: V13007Z41A

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.