KENDRA SKIN PROTECTION AND PAIN RELIEF FOR HAIR REMOVAL- lanolin, petrolatum and lidocaine 
Natureplex, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Kendra SKIN PROTECTION & PAIN RELIEF FOR HAIR REMOVAL

A&D OINTMENT

Drug Facts

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

Use

Warnings

For external use only

When using this product

  • do not get into eyes

Stop use and ask a doctor if

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

Do not use on

  • deep or puncture wounds
  • animal bites
  • serious burns

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

Directions

Other information

Inactive ingredients

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

Questions or Comments?

1-866-323-0107 or www.kendracollection.com

4% LIDOCAINE

Drug Facts

Active ingredient

Lidocaine 4%

Purpose

Pain Relieving Cream

Use

Warnings

For external use only

Avoid contact with the eyes

Do Not Use

  • 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

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

Stop use and ask a doctor if

  • 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

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

Directions

Other information

Inactive ingredients

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

Questions or Comments?

1-866-323-0107 or www.kendracollection.com

This product
is manufactured
and distributed
by Natureplex™.

PRINCIPAL DISPLAY PANEL - Kit Carton

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
KENDRA SKIN PROTECTION AND PAIN RELIEF FOR HAIR REMOVAL 
lanolin, petrolatum and lidocaine kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67234-048
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67234-048-011 in 1 CARTON06/04/2003
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 TUBE 28 g
Part 21 TUBE 28 g
Part 1 of 2
A AND D 
lanolin and petrolatum ointment, augmented
Product Information
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Lanolin (UNII: 7EV65EAW6H) (Lanolin - UNII:7EV65EAW6H) Lanolin155 mg  in 1 g
Petrolatum (UNII: 4T6H12BN9U) (Petrolatum - UNII:4T6H12BN9U) Petrolatum534 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
YELLOW WAX (UNII: 2ZA36H0S2V)  
COD LIVER OIL (UNII: BBL281NWFG)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
128 g in 1 TUBE; Type 8: Possible Combination Based on Cross Labeling of Separate Products (Temporary Type)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34706/04/2003
Part 2 of 2
LIDOCAINE PAIN RELIEVING 
lidocaine cream
Product Information
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Lidocaine (UNII: 98PI200987) (Lidocaine - UNII:98PI200987) Lidocaine40 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
SULISOBENZONE (UNII: 1W6L629B4K)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
DIMETHYL SULFOXIDE (UNII: YOW8V9698H)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
ARGININE (UNII: 94ZLA3W45F)  
WATER (UNII: 059QF0KO0R)  
JOJOBA OIL (UNII: 724GKU717M)  
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TEA TREE OIL (UNII: VIF565UC2G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
128 g in 1 TUBE; Type 8: Possible Combination Based on Cross Labeling of Separate Products (Temporary Type)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34812/25/2009
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34706/04/2003
Labeler - Natureplex, LLC (062808196)
Establishment
NameAddressID/FEIBusiness Operations
Natureplex LLC062808196MANUFACTURE(67234-048)

Revised: 10/2017
Document Id: e248765f-837d-4db7-96a3-7ac5f0795318
Set id: e422a3ad-9208-41ab-9dc7-9af81f059eae
Version: 3
Effective Time: 20171020
 
Natureplex, LLC