TATTOO AFTER CARE  A AND D- lanolin and petrolatum ointment 
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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Tattoo After Care
A&D Ointment

Drug Facts

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

Uses

Warnings

For external use only.

When using this product

  • do not get into eyes

Stop use and ask a doctor if

  • condition worsens
  • symptoms last 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 right away: 800-222-1222.

Direction

Other information

Inactive ingredients

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

Questions or Comments?

866-323-0107 or www.natureplex.com

*This product is manufactured and distributed by Natureplex™.

PRINCIPAL DISPLAY PANEL - 42.5 g Tube Carton

NDC# 67234-066-01

Natureplex

TATTOO
AFTER
CARE

A&D OINTMENT
SKIN PROTECTANT

NET WT. 1.5 Oz. (42.5g)

For additional stability, this carton is
larger than the tube

Principal Display Panel - 42.5 g Tube Carton
TATTOO AFTER CARE   A AND D
lanolin and petrolatum ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67234-066
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Lanolin (UNII: 7EV65EAW6H) (Lanolin - UNII:7EV65EAW6H) Lanolin0.15 mg  in 1 g
Petrolatum (UNII: 4T6H12BN9U) (Petrolatum - UNII:4T6H12BN9U) Petrolatum0.53 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WHITE WAX (UNII: 7G1J5DA97F)  
COD LIVER OIL (UNII: BBL281NWFG)  
MINERAL OIL (UNII: T5L8T28FGP)  
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67234-066-011 in 1 CARTON06/15/2018
142.5 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34706/15/2018
Labeler - Natureplex LLC (062808196)
Establishment
NameAddressID/FEIBusiness Operations
Natureplex LLC062808196MANUFACTURE(67234-066)

Revised: 4/2018
Document Id: 9d172c92-66eb-4878-b8ce-0df110014e85
Set id: e12667d7-31a4-4a15-a7de-8f46191f80e3
Version: 1
Effective Time: 20180406
 
Natureplex LLC