NEUTRACETT
- Manufacturer
- ADVANCED BIOMEDICS INC | COSMETIC ENTERPRISES LTD
- Effective date
- 2010-08-10
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:25:30
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Water (Aqua), Neutracett Complex (Hyaluronic Acid, DL Panthenol), PPG-5-Ceteth-20, Ammonium Acryloyldimethyltaurate/VP Copolymer, Phenoxyethanol, Chlorphenesin, Benzoic Acid.
OTC - ACTIVE INGREDIENT SECTION
Active ingredients/Purpose
Allantoin 0.5% Skin Protectant
Glycerin 5.0% Skin Protectant
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have: *serious burns * deep or puncture wounds * animal bites
Questions? 800-833-4164
www.neutracett.com Patents
Pending
OTC - DO NOT USE SECTION
Do not use: *if you are allergic to any of the ingredients *avoid contact with the eyes
OTC - STOP USE SECTION
Stop use and ask a doctor: * if condition worsens or does not improve after 7 days * if rash or other allergic reactions occur
OTC - PURPOSE SECTION
Uses: Soothes, protects and eases skin trauma for tattoo application or removal.
WARNINGS SECTION
DOSAGE & ADMINISTRATION SECTION
Directions: Gently clean area with mild cleanser. Apply gel to entire area 3-4 times per day or as directed. May be covered with sterile bandage. See website for more information.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Neutracett
Aid 4-Healing
Skin Recovery Treatment
For Tattoo, tattoo removal
All natural / won’t stain
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1045324 | allantoin 0.5 % / glycerin 5 % Topical Gel | PSN | 1 |
| 1045328 | Neutracett 0.5 % / 5 % Topical Gel | PSN | 1 |
| 1045328 | allantoin 0.005 MG/MG / glycerin 0.05 MG/MG Topical Gel [Neutracett] | SBD | 1 |
| 1045324 | allantoin 0.005 MG/MG / glycerin 0.05 MG/MG Topical Gel | SCD | 1 |
| 1045328 | Neutracett (allantoin 0.5 % / glycerin 5 % ) Topical Gel | SY | 1 |
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| GLYCERIN Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| c6f86816-7da6-43ea-8c25-ac9758311cc5 | Product name | 1 | 20220118 |
| 252e11b6-1a9a-4283-a242-df2c129c496d | Product name | 3 | 20170717 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 51435-002-01 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-c46b-621f-e053-dbdaa90a74ad | TUBE LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51435-002-01 | NEUTRACETTTATTOO | 28.3 g in 1 TUBE | GEL | 28.3 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ALLANTOIN | ACTIVE INGREDIENT | 344S277G0Z | 1 | |
| GLYCERIN | ACTIVE INGREDIENT | PDC6A3C0OX | 1 | |
| ALLANTOIN | ACTIVE MOIETY | 344S277G0Z | 1 | |
| GLYCERIN | ACTIVE MOIETY | PDC6A3C0OX | 1 | |
| BENZOIC ACID | INACTIVE INGREDIENT | 8SKN0B0MIM | 1 | |
| CHLORPHENESIN | INACTIVE INGREDIENT | I670DAL4SZ | 1 | |
| HYALURONIC ACID | INACTIVE INGREDIENT | S270N0TRQY | 1 | |
| PANTHENOL | INACTIVE INGREDIENT | WV9CM0O67Z | 1 | |
| PHENOXYETHANOL | INACTIVE INGREDIENT | HIE492ZZ3T | 1 | |
| PPG-5-CETETH-20 | INACTIVE INGREDIENT | 4AAN25P8P4 | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- NEUTRACETT TATTOO
- ALLANTOIN GLYCERIN
- ALLANTOIN
- GLYCERIN
- WATER
- HYALURONIC ACID
- PANTHENOL
- PPG-5-CETETH-20
- PHENOXYETHANOL
- CHLORPHENESIN
- BENZOIC ACID
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 51435-002 | 51435-002-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALLANTOIN | 344S277G0Z | ACTIB |
| GLYCERIN | PDC6A3C0OX | ACTIB |
| WATER | 059QF0KO0R | IACT |
| HYALURONIC ACID | S270N0TRQY | IACT |
| PANTHENOL | WV9CM0O67Z | IACT |
| PPG-5-CETETH-20 | 4AAN25P8P4 | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| CHLORPHENESIN | I670DAL4SZ | IACT |
| BENZOIC ACID | 8SKN0B0MIM | IACT |
Source Document#
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| PHENOXYETHANOL | PHENOXYETHANOL | HIE492ZZ3T | GEL / TOPICAL | 14 mg | ||
| PHENOXYETHANOL | PHENOXYETHANOL | HIE492ZZ3T | AEROSOL, FOAM / TOPICAL | 72 mg | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | INJECTION / INTRAVENOUS | 5 %w/v | ||
| PHENOXYETHANOL | PHENOXYETHANOL | HIE492ZZ3T | CREAM / TOPICAL | 57 mg | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | AEROSOL, FOAM / TOPICAL | 1 mg | ||
| PHENOXYETHANOL | PHENOXYETHANOL | HIE492ZZ3T | AEROSOL / TOPICAL | 1.05 %w/w | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | MOUTHWASH / BUCCAL | NA | ||
| PHENOXYETHANOL | PHENOXYETHANOL | HIE492ZZ3T | CREAM, AUGMENTED / TOPICAL | 10 mg | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | TABLET, COATED / ORAL | NA | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | CONCENTRATE / ORAL | 12.5 mg/5ml | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | GEL / TOPICAL | 0.1 %w/w | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | TABLET, FILM COATED / ORAL | NA | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | SOLUTION / ORAL | 100 mg | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | SUSPENSION / ORAL | 15 mg | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | CREAM / VAGINAL | 10 mg | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | INJECTION / INTRAMUSCULAR | 5 %w/v | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | INJECTION, SOLUTION / INTRAMUSCULAR | 0.2 %w/v | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | ELIXIR / ORAL | 90 mg | ||
| PHENOXYETHANOL | PHENOXYETHANOL | HIE492ZZ3T | LOTION / TOPICAL | 1 %w/w | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | SUPPOSITORY / VAGINAL | 2 mg | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | SYRUP / ORAL | 20 mg | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | CREAM / TOPICAL | 6 mg | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | SOLUTION / TOPICAL | 0.1 %w/w | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | SOLUTION / IRRIGATION | 0.02 %w/v | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | LIQUID / ORAL | 2 mg/1ml | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | AEROSOL, FOAM / VAGINAL | 0.1 %w/w | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | SUSPENSION / RECTAL | 0.1 %w/w | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | LOTION / TOPICAL | 0.2 %w/w | ||
| BENZOIC ACID | BENZOIC ACID | 8SKN0B0MIM | GEL / RECTAL | 11 mg |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| cdf18699-0fa4-416f-ba57-a4519713ee71 | 423dea3d-c2a1-4bc2-a628-9836e0ff9c58 | 2010-08-10 | Warnings | cdf18699-0fa4-416f-ba57-a4519713ee71 423dea3d-c2a1-4bc2-a628-9836e0ff9c58 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
