FDA.reportPublic FDA data

Tattoo After Care A&D Ointment

Manufacturer
Natureplex LLC
Effective date
2018-04-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:55:56

Label at a glance#

ProductTattoo After Care A and D
Active ingredientLanolin, Petrolatum
Label structure10 sections

Indications and uses

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

Storage and handling

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

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

Uses

INDICATIONS & USAGE SECTION

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

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 last 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 right away: 800-222-1222.

Direction

DOSAGE & ADMINISTRATION SECTION

  • For skin protectant use: apply as needed

Other information

STORAGE AND HANDLING SECTION

  • 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

INACTIVE INGREDIENT SECTION

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

SPL UNCLASSIFIED SECTION

*This product is manufactured and distributed by Natureplex™.

PRINCIPAL DISPLAY PANEL - 42.5 g Tube Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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
Principal Display Panel - 42.5 g Tube Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
664981lanolin 15.5 % / petrolatum 53.4 % Topical OintmentPSN1
664981lanolin 0.155 MG/MG / petrolatum 0.534 MG/MG Topical OintmentSCD1
664981lanolin 15.5 % / petrolatum 53.4 % Topical OintmentSY1
664981lanolin 15.5 GM per 100 GM / petrolatum 53.4 GM per 100 GM Topical OintmentSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
67234-066-012025-01-30C16284748780-12cef2736-9931-d83d-e063-dadaa90ab31fTattoo After Care A&D Ointment

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67234-066-01Tattoo After Care A and D42.5 g in 1 TUBEOINTMENT42.51
67234-066-01Tattoo After Care A and D1 in 1 CARTONOINTMENT11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67234-066TATTOO AFTER CARE A AND D (LANOLIN AND PETROLATUM) OINTMENT [NATUREPLEX LLC]1Legacy NDC, 2 package rows20180615_e12667d7-31a4-4a15-a7de-8f46191f80e3.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67234-06667234-066-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
Lanolin7EV65EAW6HACTIB
Petrolatum4T6H12BN9UACTIB
WHITE WAX7G1J5DA97FIACT
COD LIVER OILBBL281NWFGIACT
MINERAL OILT5L8T28FGPIACT
MICROCRYSTALLINE WAXXOF597Q3KYIACT

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
9d172c92-66eb-4878-b8ce-0df110014e85e12667d7-31a4-4a15-a7de-8f46191f80e32018-04-06WarningsExact identifier
spl id: 9d172c92-66eb-4878-b8ce-0df110014e85
spl set id: e12667d7-31a4-4a15-a7de-8f46191f80e3

Reported adverse events (FAERS/openFDA)#

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