Nadinola Skin Fade Cream for Normal Skin

Manufacturer
J. Strickland & Co.
Effective date
2018-01-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:04:45

Label at a glance#

ProductNadinola Skin Fade for Normal Skin
Active ingredientHYDROQUINONE, OCTISALATE
Label structure6 sections

Indications and uses

Gradually fades areas of skin discoloration such as age spots  freckles  liver spots  dark areas that can occur while using oral contraceptives.

Dosage and administration

If skin is sensitive, test on a small area inside the elbow overnight before use.  Adults and children 12 years and older, apply a thin layer to affected area twice daily, or as directed by a doctor.  If going outside, use a sunscreen or wear protective clothing. Children under 12 years of age, ask a doctor before use.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Hydroquinone, 2%; Octisalate, 3%

Skin Lightener Sunscreen

OTC - PURPOSE SECTION

Uses:

INDICATIONS & USAGE SECTION

Gradually fades areas of skin discoloration such as

  • age spots 
  • freckles 
  • liver spots 
  • dark areas that can occur while using oral contraceptives.

Warnings:

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • on inflamed or broken skin 
  • to prevent sunburn
  • if product is tan or brown.

When using this product,

OTC - WHEN USING SECTION

  • mild irritation may occur 
  • avoid contact with eyes. If contact occurs, rinse with water.
  • avoid unnecessary sun exposure and use a sunscreen or protective clothing

Stop use and consult a doctor if

OTC - STOP USE SECTION

  • a gradual blue-black darkening of the skin occurs
  • irritation becomes severe 
  • no improvement is seen after 3 months

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

consult a health professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Directions:

DOSAGE & ADMINISTRATION SECTION

  • If skin is sensitive, test on a small area inside the elbow overnight before use. 
  • Adults and children 12 years and older, apply a thin layer to affected area twice daily, or as directed by a doctor. 
  • If going outside, use a sunscreen or wear protective clothing.
  • Children under 12 years of age, ask a doctor before use.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

water, glyceryl stearate, PEG-8, isopropyl myristate, isopropyl isostearate, cetyl alcohol, PEG-100 stearate, fragrance, citric acid, methylparaben, propylparaben, sodium bisulfite.

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

12022-015-0012022-015-00

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
12022-01512022-015-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
b34c925f-dbd9-5030-e053-2a95a90a19ea31660fbf-cbc8-4ca5-96d9-376e2a4da94e2020-11-04WarningsExact identifier
spl set id: 31660fbf-cbc8-4ca5-96d9-376e2a4da94e

Reported adverse events (FAERS/openFDA)#

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