Kendra Skin Protection And Pain Relief For Hair Removal
FDA Label NDC 67234-048

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Natureplex, Llc for the product Kendra Skin Protection And Pain Relief For Hair Removal (NDC 67234-048). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding other, otc - purpose, use, warnings, when using this product, stop use and ask a doctor if, do not use on, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

A&D OINTMENT

Drug Facts

4% LIDOCAINE

Drug Facts

This product
is manufactured
and distributed
by Natureplex™.

Otc - Purpose

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

Use

  • temporarily protects and helps relieve minor skin irritation due to tattooing, piercing, and hair removal
    • for temporary relief of pain associated with minor skin irritations due to tattooing, piercing, and hair removal

Warnings

For external use only

For external use only

Avoid contact with the eyes

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
    • 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

Do Not Use On

  • deep or puncture wounds
  • animal bites
  • serious burns

Otc - Keep Out Of Reach Of Children

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

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

Directions

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

  • 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
    • 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

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

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

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

Active Ingredient

Lidocaine 4%

Purpose

Pain Relieving Cream

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

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)

Principal Display Panel (Kit Carton)

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