TATTOO AFTER CARE A AND D- lanolin and petrolatum ointment

Tattoo After Care by

Drug Labeling and Warnings

Tattoo After Care by is a Otc medication manufactured, distributed, or labeled by Natureplex LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredients	Purpose
Lanolin 15.5%	Skin protectant
Petrolatum 53.4%	Skin protectant

Uses

• temporarily protects minor:
  • cuts
  • scrapes
  • burns
• temporarily protects chapped or cracked skin and lips

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

• For skin protectant use: apply as needed

Other information

• store at 15 to 30°C (59 to 86°F)
• Tamper Evident: DO NOT USE IF SAFETY SEAL ON TUBE IS BROKEN OR MISSING

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

SPL UNCLASSIFIED SECTION

*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

INGREDIENTS AND APPEARANCE

TATTOO AFTER CARE   A AND D
lanolin and petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67234-066
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Lanolin (UNII: 7EV65EAW6H) (Lanolin - UNII:7EV65EAW6H)	Lanolin	0.15 mg  in 1 g
Petrolatum (UNII: 4T6H12BN9U) (Petrolatum - UNII:4T6H12BN9U)	Petrolatum	0.53 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WHITE WAX (UNII: 7G1J5DA97F)
COD LIVER OIL (UNII: BBL281NWFG)
MINERAL OIL (UNII: T5L8T28FGP)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67234-066-01	1 in 1 CARTON	06/15/2018
1		42.5 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	06/15/2018

Labeler - Natureplex LLC (062808196)

Establishment
Name	Address	ID/FEI	Business Operations
Natureplex LLC		062808196	MANUFACTURE(67234-066)