Supernova Lab Pure Orange

Manufacturer
Supernova Coating, S.A. de C.V.
Effective date
2020-05-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:15:04

Label at a glance#

ProductSupernova Lab Pure Orange
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing. Other information Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

  • in children less than 2 months of age
  • on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbomer, Distilled Water, Triethanolamine, Aloe Vera and Essential Oils.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76726-002-01Supernova Lab Pure Orange120 mL in 1 BOTTLE, PLASTICGEL1201
76726-002-02Supernova Lab Pure Orange250 mL in 1 BOTTLE, PLASTICGEL2501
76726-002-03Supernova Lab Pure Orange500 mL in 1 BOTTLE, PLASTICGEL5001
76726-002-04Supernova Lab Pure Orange1000 mL in 1 BOTTLE, PLASTICGEL10001
76726-002-05Supernova Lab Pure Orange20000 mL in 1 BOTTLE, PLASTICGEL200001
76726-002-06Supernova Lab Pure Orange1000000 mL in 1 BOTTLE, PLASTICGEL10000001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76726-002SUPERNOVA LAB PURE ORANGE (ALCOHOL) GEL [SUPERNOVA COATING, S.A. DE C.V.]1Legacy NDC, 6 package rows20200529_3d9c4a72-0c02-484a-a6a4-2e10485ed3b7.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76726-00276726-002-01, 76726-002-02, 76726-002-03, 76726-002-04, 76726-002-05, 76726-002-06

Ingredients#

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

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

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
6883a2c1-2588-45a7-ade9-3338693cafb43d9c4a72-0c02-484a-a6a4-2e10485ed3b72020-05-28WarningsExact identifier
spl id: 6883a2c1-2588-45a7-ade9-3338693cafb4
spl set id: 3d9c4a72-0c02-484a-a6a4-2e10485ed3b7

Reported adverse events (FAERS/openFDA)#

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