ACTIVE AGAIN

Manufacturer
Hope Science Inc
Effective date
2021-07-11
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 22:41:03

Label at a glance#

ProductACTIVE AGAIN
Active ingredientMENTHOL
Label structure10 sections

Dosage and administration

Adults and children 2 yrs. of age and older, apply to affected area not more than 3 to 4 times a day. Children under 2 yrs. of age, consult a physician.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

MENTHOL (1.25%)

PURPOSE

OTC - PURPOSE SECTION

TOPICAL ANALGESIC

INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, and sprains.

WARNINGS:

WARNINGS SECTION

  • For external use only.
  • Avoid contact with eyes.
  • If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of product and consult a physician.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If swallowed, get medical help or contact a poison control center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 yrs. of age and older, apply to affected area not more than 3 to 4 times a day. Children under 2 yrs. of age, consult a physician.

OTHER INFORMATION:

OTHER SAFETY INFORMATION

Store in a cool, dry place.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Benzyl Alcohol, Caprylyl Glycol, Citric Acid, Esterified Fatty Acids (EFAC Proprietary Blend), Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Hexylene Glycol, Lecithin, Mentha Piperita (Peppermint) Oil, PEG-100
Stearate, Phenoxyethanol, Sodium Hydroxide, Tocopheryl Acetate, Water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Active Again_Hope Science_LBL_16ozActive Again_Hope Science_LBL_16oz

Active Again_Hope Science_LBL_4ozActive Again_Hope Science_LBL_4oz

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71970-30371970-303-45, 71970-303-49
65643-304

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 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
f8368eb9-a1da-654b-e053-6294a90a45825a6b1789-26e2-4cb7-a78d-47917d7b22eb2023-03-31WarningsExact identifier
spl set id: 5a6b1789-26e2-4cb7-a78d-47917d7b22eb

Reported adverse events (FAERS/openFDA)#

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