LubeLife Climax Control Delay

Product NDC
71683-005
Requested package NDC
71683-005-01
11-digit product format
716830005
Labeler code
71683
Product ID
71683-005_3e62265a-9563-8fee-e063-6394a90a13d4
Type
HUMAN OTC DRUG
Nonproprietary name
Benzocaine
Dosage form
SPRAY
Route
TOPICAL
Labeler
CC Wellness LLC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-01-01
Substance
BENZOCAINE
Active strength
7.5 g/100mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-288af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-081332a3947898…d4bfe170f9cd…

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
LubeLife Climax Control Delay
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZOCAINE7.5 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
U3RSY48JW5Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
e1a98e6d-0c24-75b8-e053-2a95a90ad136Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71683-005-012024-01-30C16284748780-11030e364-fc41-111a-e063-dadaa90a10e2e1a98e6d-0c24-75b8-e053-2a95a90ad136

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71683-005-01LubeLife Climax Control Delay1 in 1 BOXSPRAY13
71683-005-02LubeLife Climax Control Delay60 mL in 1 BOTTLE, PLASTICSPRAY603

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 114 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TheraCare Maximum Strength Pain Relief PatchLIDOCAINEVeridian Healthcaredfaf8a77-2276-4791-e053-2a95a90a32882024-12-10WarningsExact identifier
application number: M017
Methyl SalicylateMETHYL SALICYLATEAlexso, Inceef555d3-f23d-4847-93f3-fa7a06072a0f2024-12-09WarningsExact identifier
application number: M017
Lidocaine 4 PercentLIDOCAINESA3, LLC651710db-3c50-4bcf-b7cc-9ed24f6634272024-12-09WarningsExact identifier
application number: M017
HealthWise Pain Relief Lidocaine PatchLIDOCAINE 4%Veridian Healthcare28db1c03-d01f-83ea-e063-6294a90aee262024-12-09WarningsExact identifier
application number: M017
Joint and Muscle Pain ReliefMENTHOLAllure Labse82f99fd-c2ef-686f-e053-2a95a90a1dc92024-12-09WarningsExact identifier
application number: M017
Tough Love Pain RelievingLIDOCAINE HCLAllure Labsee8c1a2b-36ef-6fd7-e053-2a95a90a9c012024-12-09WarningsExact identifier
application number: M017
CapsaicinCAPSAICINSA3, LLC5617e91d-e650-4a0d-8565-b8288ea41c772024-12-09WarningsExact identifier
application number: M017
Medicaine Sting and BiteBENZOCAINEJames Alexander Corporation753e6cbe-31e0-4017-93d0-8b4bf5972f372024-12-09WarningsExact identifier
application number: M017
AUVON Pain Relief Roll-onMENTHOLSHENZHEN YUWEN E-COMMERCE CO., LTD.df239c4d-af6a-41ca-baed-d0788782ce9f2024-12-08WarningsExact identifier
application number: M017
AUVON Pain Relief Roll-onLIDOCAINESHENZHEN YUWEN E-COMMERCE CO., LTD.8b30f623-6077-4f2e-8fa4-ce4a298953b52024-12-08WarningsExact identifier
application number: M017
QC Medicated anti itchPRAMOXINE HYDROCHLORIDE, MENTHOLChain Drug Marketing Associationb5e41e3a-81df-3a63-e053-2a95a90a58392024-12-08WarningsExact identifier
application number: M017
QC Lidocaine Maximum StrengthLIDOCAINE HCLChain Drug Marketing Associationb5e1b1ab-8a95-2d2d-e053-2995a90aea532024-12-08WarningsExact identifier
application number: M017
CapsaicinCAPSAICINAlexso, Inc433da27d-04fb-481a-bbb0-874bb72c806a2024-12-06WarningsExact identifier
application number: M017
POMG PAIN RELIEF BODYLIDOCAINEPOMG LLC28d7ac46-b27f-43bb-e063-6294a90a93ed2024-12-06WarningsExact identifier
application number: M017
Capsaicin 0.1 PercentCAPSAICINAlexso, Inc0090ca38-6433-45c4-9453-edf2788c14c62024-12-06WarningsExact identifier
application number: M017
Signature Care MentholMENTHOL 4%Safeway27d3cb47-a6c7-5b7a-e063-6394a90a056f2024-12-05WarningsExact identifier
application number: M017
ITCH XBENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDEBF ASCHER AND CO INC03c16d33-8f59-0184-e054-00144ff8d46c2024-12-05WarningsExact identifier
application number: M017
PO First Aid Series BURNLIDOCAINE HYDROCHLORIDENantong Health & Beyond Hygienic Products Inc.f1c349a8-216d-4233-922e-c95329a33d1e2024-12-05WarningsExact identifier
application number: M017
Post Treatment BalmHYDROCORTISONEAllure Labs Inc.faa803e6-453c-4d86-85dd-5a5dcdd72d022024-12-05WarningsExact identifier
application number: M017
CBD Pain Relief CreamTROLAMINE SALICYLATEAllure Labsb6b3102a-4154-2da2-e053-2995a90ae99f2024-12-05WarningsExact identifier
application number: M017

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71683-005-01716830005011 BOTTLE, PLASTIC in 1 BOX (71683-005-01) / 60 mL in 1 BOTTLE, PLASTIC (71683-005-02) 2022-01-010000-00-00NoNoCurrent