FDA.reportPublic FDA data

Kendra SKIN PROTECTION and PAIN RELIEF FOR HAIR REMOVAL

Manufacturer
Natureplex, LLC | Natureplex LLC
Effective date
2017-10-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:52:46

Label at a glance#

ProductKendra SKIN PROTECTION and PAIN RELIEF FOR HAIR REMOVAL
Active ingredientLanolin, Petrolatum, Lidocaine
Label structure19 sections

Dosage and administration

After procedure, apply A&D Skin Protectant as needed to affected skin.

Storage and handling

see bottom of carton for lot number and expiration date store at 15 to 30°C (59 to 86°F) do not use if carton is damaged or open do not use if seal on tube is punctured or missing

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

A&D OINTMENT

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredientsPurpose
Lanolin 15.5%Skin Protectant
Petrolatum 53.4%Skin protectant

Use

INDICATIONS & USAGE SECTION

  • temporarily protects and helps relieve minor skin irritation due to tattooing, piercing, and hair removal

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within a few days

Do not use on

OTC - DO NOT USE SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help, or contact a Poison Control Center immediately: 1-800-222-1222.

Directions

DOSAGE & ADMINISTRATION SECTION

  • After procedure, apply A&D Skin Protectant as needed to affected skin.

Other information

STORAGE AND HANDLING SECTION

  • see bottom of carton for lot number and expiration date
  • store at 15 to 30°C (59 to 86°F)
  • do not use if carton is damaged or open
  • do not use if seal on tube is punctured or missing

Inactive ingredients

INACTIVE INGREDIENT SECTION

beeswax, cod liver oil (contains vitamin A & vitamin D), fragrance, light mineral oil, microcrystalline wax

SPL UNCLASSIFIED SECTION

4% LIDOCAINE

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Purpose

OTC - PURPOSE SECTION

Pain Relieving Cream

Use

INDICATIONS & USAGE SECTION

  • for temporary relief of pain associated with minor skin irritations due to tattooing, piercing, and hair removal

Warnings

WARNINGS SECTION

For external use only

Avoid contact with the eyes

Do Not Use

OTC - DO NOT USE SECTION

  • if you are allergic to any ingredient in lidocaine cream or to similar medicines (e.g., local anesthetics such as benzocaine)
  • in large quantities, particularly over raw surfaces or blistered areas

Ask a doctor before use

OTC - ASK DOCTOR SECTION

  • if you have had an allergic reaction (e.g., rash, hives, dizziness) to any anesthetic medicine

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • you develop a persistent rash
  • conditions worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help, or contact a Poison Control Center immediately: 1-800-222-1222.

Directions

DOSAGE & ADMINISTRATION SECTION

  • For adult use only.
  • Before procedure, apply a small amount of pain relieving cream to affected area, and allow to dry. Application may be repeated up to 4 times daily.

Other information

STORAGE AND HANDLING SECTION

  • see bottom of carton for lot number and expiration date
  • store at 15 to 30°C (59 to 86°F)
  • do not use if carton is damaged or open
  • do not use if seal on tube is punctured or missing

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf juice, benzophenone-4, cetyl alcohol, dimethyl sulfoxide, jeecide cap-5, L-arginine, purified water, simmondsia chinesis (jojoba) seed oil, sodium polyacrylate, stearic acid, tea tree oil

SPL UNCLASSIFIED SECTION

This product
is manufactured
and distributed
by Natureplex™.

PRINCIPAL DISPLAY PANEL - Kit Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC# 67234-048-01

KENDRA

PAIN RELIEF & SKIN PROTECTANT

A&D OINTMENT SKIN PROTECTANT
1 TUBE NET WT. 1.75 Oz. (49.6g)

LIDOCAINE 4% PAIN RELIEVING CREAM
1 TUBE NET WT. 1.75 Oz. (49.6g)

PRINCIPAL DISPLAY PANEL - Kit Carton
PRINCIPAL DISPLAY PANEL - Kit Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
664981lanolin 15.5 % / petrolatum 53.4 % Topical OintmentPSN3
1421893lidocaine 4 % Topical CreamPSN3
664981lanolin 0.155 MG/MG / petrolatum 0.534 MG/MG Topical OintmentSCD3
1421893lidocaine 40 MG/ML Topical CreamSCD3
664981lanolin 15.5 % / petrolatum 53.4 % Topical OintmentSY3
664981lanolin 15.5 GM per 100 GM / petrolatum 53.4 GM per 100 GM Topical OintmentSY3
1421893lidocaine 4 % Topical CreamSY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
67234-048-012025-01-30C16284748780-12cef2736-6b09-d83d-e063-dadaa90ab31fKendra SKIN PROTECTION & PAIN RELIEF FOR HAIR REMOVAL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67234-048-01Kendra SKIN PROTECTION and PAIN RELIEF FOR HAIR REMOVAL1 in 1 CARTONKIT13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67234-048KENDRA SKIN PROTECTION AND PAIN RELIEF FOR HAIR REMOVAL (LANOLIN, PETROLATUM AND LIDOCAINE) KIT [NATUREPLEX, LLC]3Legacy NDC, 1 package rows20171024_e422a3ad-9208-41ab-9dc7-9af81f059eae.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67234-04867234-048-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
Lanolin7EV65EAW6HACTIB
Petrolatum4T6H12BN9UACTIB
YELLOW WAX2ZA36H0S2VIACT
COD LIVER OILBBL281NWFGIACT
LIGHT MINERAL OILN6K5787QVPIACT
MICROCRYSTALLINE WAXXOF597Q3KYIACT
Lidocaine98PI200987ACTIB
ALOE VERA LEAFZY81Z83H0XIACT
SULISOBENZONE1W6L629B4KIACT
CETYL ALCOHOL936JST6JCNIACT
DIMETHYL SULFOXIDEYOW8V9698HIACT
CAPRYLYL GLYCOL00YIU5438UIACT
ARGININE94ZLA3W45FIACT
WATER059QF0KO0RIACT
JOJOBA OIL724GKU717MIACT
SODIUM POLYACRYLATE (2500000 MW)05I15JNI2JIACT
STEARIC ACID4ELV7Z65APIACT
TEA TREE OILVIF565UC2GIACT

Source Document#

Source XML

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 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e248765f-837d-4db7-96a3-7ac5f0795318e422a3ad-9208-41ab-9dc7-9af81f059eae2017-10-20WarningsExact identifier
spl id: e248765f-837d-4db7-96a3-7ac5f0795318
spl set id: e422a3ad-9208-41ab-9dc7-9af81f059eae

Reported adverse events (FAERS/openFDA)#

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