FDA.reportPublic FDA data

Bliss Gel

Manufacturer
ExcelAg, Corp.
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:17:22

Label at a glance#

ProductBliss
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Apply liberally to palms of hands and rub until dry. Children under 6 should only use this product with adult supervision.

Storage and handling

Store this container below 104F (40C). May cause discoloration to some fabrics.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% w/w. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Sanitizer to help decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only. Keep out of reach of children. Flammable, keep away from fire or flame. When using this product keep out of eyes. In case of contact, rinse eyes with water to remove. Stop use and ask doctor if rash occurs. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally to palms of hands and rub until dry. Children under 6 should only use this product with adult supervision.

Other information

STORAGE AND HANDLING SECTION

  • Store this container below 104F (40C).
  • May cause discoloration to some fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, citric acid, lemon oil, lavender oil, glycerin, polyethylene glycol

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

236 mL NDC: 74880-200-08

Bliss Gel 8 ozBliss Gel 8 oz473 mL NDC: 74880-200-16

Bliss Gel 16 oz RefillBliss Gel 16 oz Refill

3785 mL NDC: 74880-200-01

Bliss Gel 128 ozBliss Gel 128 oz60 mL NDC: 74880-100-02

Bliss 2 ozBliss 2 oz118 mL NDC: 74880-100-04

Bliss 4 ozBliss 4 oz236 mL NDC: 74880-100-08

Bliss 8 ozBliss 8 oz473 mL NDC: 74880-100-16

Bliss 16 oz FrontBliss 16 oz Front

Bliss 16 oz BackBliss 16 oz Back

473 mL NDC: 74880-100-17

Bliss 16 oz RefillBliss 16 oz Refill3785 mL NDC: 74880-100-01

Bliss 128 ozBliss 128 oz

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74880-20074880-200-02, 74880-200-04, 74880-200-08, 74880-200-16, 74880-200-01
74880-10074880-100-02, 74880-100-04, 74880-100-08, 74880-100-16, 74880-100-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
LAVENDER OILZBP1YXW0H8IACT
LEMON OILI9GRO824LLIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
ALCOHOL3K9958V90MACTIB
POLYETHYLENE GLYCOL 1000U076Q6Q621IACT
LAVENDER OILZBP1YXW0H8IACT
LEMON OILI9GRO824LLIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
ALCOHOL3K9958V90MACTIB

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
e77681cd-1746-269e-e053-2a95a90a1e01a615f93b-5122-53de-e053-2995a90ab7e32022-08-30WarningsExact identifier
spl set id: a615f93b-5122-53de-e053-2995a90ab7e3

Reported adverse events (FAERS/openFDA)#

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