FDA.reportPublic FDA data

Renuu NL

Manufacturer
Patchwerx Labs
Effective date
2015-05-28
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:20:51

Label at a glance#

ProductRenuu NL
Active ingredientALLANTOIN, PETROLATUM
Label structure9 sections

Storage and handling

Other information store below 25 C (77 F). avoid direct sunlight

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

Other Ingredients vitamin E, Lidocaine, onion extract

DESCRIPTION SECTION

Active Ingredient

Allantoin 2.00 %

Petrolatum 30.00 %

DESCRIPTION SECTION

Purpose

Skin Protectant

Topical Anesthetic

Skin Protectant

INDICATIONS & USAGE SECTION

Uses

- Scar Management - Temporarily protects minor cuts , scrapes and burns

- Temporary relief of pain associated with minor cuts, scrapes and minor skin irritations

WARNINGS SECTION

For external use only

Do not use

- on deep or puncture wounds, animal bites, serious burns

- in large quantities, particularly over raw surfaces or blistered areas

When using this product

- avoid contact with 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

Keep out of reach of children. If pregnant or breastfeeding, contact physician prior to use

DOSAGE & ADMINISTRATION SECTION

Directions

How to apply - clean and dry affected area - remove mesh from backing and apply to affected area

- use only one mesh at a time, and maximum of four mesh / day - leave mesh on affected area for up to

8 hours - children under 12 should consult

physician prior to use

STORAGE AND HANDLING SECTION

Other information store below 25 C (77 F). avoid direct sunlight

SPL UNCLASSIFIED SECTION

For questions or concerns about this product, please call us - weekdays from 9 AM to 5 PM PST (1) 800-590-8070

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

renuu_nl_low_res_flat.jpgrenuu_nl_low_res_flat.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1651594allantoin 2 % / petrolatum 30 % Medicated PatchPSN1
1651594allantoin 0.02 MG/MG / petrolatum 0.3 MG/MG Medicated PatchSCD1
1651594allantoin 2 % / petrolatum 30 % Medicated PatchSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69329-011-152020-01-31C16284748780-19d75b9d0-c97c-f424-e053-dadaa90a57ceRENUU NL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69329-011-01Renuu NL100 g in 1 PATCHPATCH1001
69329-011-15Renuu NL15 in 1 BOXPATCH151

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69329-011RENUU NL (ALLANTOIN, PETROLATUM) PATCH [PATCHWERX LABS]1Legacy NDC, 2 package rows20150529_172e582c-7e76-38ac-e054-00144ff88e88.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69329-011-15EA - Each69329-01124c27948-5121-4ec2-9185-a4c662d23db512015-10-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALLANTOINACTIVE INGREDIENT344S277G0Z1
PETROLATUMACTIVE INGREDIENT4T6H12BN9U1
ALLANTOINACTIVE MOIETY344S277G0Z1
PETROLATUMACTIVE MOIETY4T6H12BN9U1
.ALPHA.-TOCOPHEROLINACTIVE INGREDIENTH4N855PNZ11
ONIONINACTIVE INGREDIENT492225Q21H1

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69329-01169329-011-01, 69329-011-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
ONION492225Q21HIACT
ALLANTOIN344S277G0ZACTIB
PETROLATUM4T6H12BN9UACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 10 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
.ALPHA.-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1TABLET / ORAL2 mgExact identifier — unii candidate
10 equally ranked IID candidates
.ALPHA.-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1SOLUTION / ORAL1.05 mg/1mlExact identifier — unii candidate
10 equally ranked IID candidates
.ALPHA.-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1TABLET, CHEWABLE / ORAL0.1 mgExact identifier — unii candidate
10 equally ranked IID candidates
.ALPHA.-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1TABLET, EXTENDED RELEASE / ORAL4 mgExact identifier — unii candidate
10 equally ranked IID candidates
.ALPHA.-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1TABLET, FILM COATED / ORAL246 mgExact identifier — unii candidate
10 equally ranked IID candidates
.ALPHA.-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1OINTMENT / TOPICALNAExact identifier — unii candidate
10 equally ranked IID candidates
.ALPHA.-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1FILM, SOLUBLE / BUCCAL0.07 mgExact identifier — unii candidate
10 equally ranked IID candidates
.ALPHA.-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS0.64 mgExact identifier — unii candidate
10 equally ranked IID candidates
.ALPHA.-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1CAPSULE / ORAL16 mgExact identifier — unii candidate
10 equally ranked IID candidates
.ALPHA.-TOCOPHEROL.ALPHA.-TOCOPHEROLH4N855PNZ1SYSTEM / TOPICAL0.1 mgExact identifier — unii candidate
10 equally ranked IID candidates

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
172e582c-7e77-38ac-e054-00144ff88e88172e582c-7e76-38ac-e054-00144ff88e882015-05-28WarningsExact identifier
spl id: 172e582c-7e77-38ac-e054-00144ff88e88
spl set id: 172e582c-7e76-38ac-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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