Indications and uses
Gradually fades skin discolorations in dark areas, age spots, freckles, liver spots and dark areas that can occur while using oral contraceptives
Gradually fades skin discolorations in dark areas, age spots, freckles, liver spots and dark areas that can occur while using oral contraceptives
• If skin is sensitive, test on a small area inside the elbow overnight before use. • adults and children 12 years and older apply as a thin layer to affected area twice daily or as directed by a doctor. • Children under 12 years of age ask a doctor before use.
Hydroquinone 2%
Ethylhexyl Methoxycinnamate 3%
Hydroquinone 2% ............................... Skin Lightener
Ethylhexyl Methoxycinnamate 3% ..... Sunscreen
Gradually fades skin discolorations in dark areas, age spots, freckles, liver spots and dark areas that can occur while using oral contraceptives
For external use only
To prevent sunburn • On inflamed or broken skin
• 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
• A gradual blue-black darkening of the skin ocurs
• Irritation becomes severe
• No improvement is seen after 3 months
consult a health professional before use.
In case of accidental ingestion, get medical help or contact a poison control center immediately.
• If skin is sensitive, test on a small area inside the elbow overnight before use.
• adults and children 12 years and older apply as a thin layer to affected area twice daily or as directed by a doctor.
• Children under 12 years of age ask a doctor before use.
Water (Aqua), Coco-Caprylate/Caprate, Stearic Acid, PEG-8, Cetyl Alcohol, Stearyl Stearate, Glyceryl Stearate, PEG-100, Propylene Glycol, Kojic Acid, Daucus Carota Sative (Carrot) Seed Oil, Vaccinium Myrtillus Extract, Saccharum Officinarum (Sugar Cane) Extract, Acer Saccharum (Sugar Maple) Extract, Citrus Aurantium Dulcis (Orange) Fruit Extract, Citrus Medica Limonum (Lemon) Fruit Extract, Pentetic Acid, Zea Mays (Corn) Oil, Xanthan Gum, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate (Vitamin A), Beta-Carotene, Sodium Sulfite, Sodium Metabisulfite, Tetrasodium EDTA, Methylparaben, Propylparaben, DMDM Hydantoin, Fragrance (Parfum)
Total White
Brightening Body Cream
Lightens Skin
Natural Bio-vegetal Activation
With Carrot Oil
8 OZ e 227 g Distributed by Heaven Scent, Miami FL
shimonb@yzyinc.com 877-999-3534
Tottenham, London N17 OQT, UK
MADE IN USA

Total White
Brightening Body Cream

Total White Brightening Cream diminishes the appearance of dark spots and skin discolorations caused by acne, aging, sun damage and pregnancey. This rich cream is formulated with Carrot Oil and Vitamins A and E; it effectivly moisturizes and nourishes your skin, while it protects from future damage. It safely brightens and evens dark spots for younger, healthier, more radiant looking skin.

Total White Brightening Body Cream diminishes the appearance of dark spots and skin discolorations caused by acne, aging, sun damage, and pregnancy. This rich cream is formulated with Carrot Oil and Vitamins A and E, it effectively moisturizes and nourishes your skin, while it protects against future damage. It safely brightens and evens dark spots for younger, healthier more radiant looking skin.

Total White Brightening Body Cream With carrot oil Lightens SkinNatural Bio-Vegetal Activator

| Class | Version | Type | Effective |
|---|---|---|---|
| HYDROQUINONE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 85490a6b-2306-6bf2-c51b-eb63537dc2da | Product name | 1 | 20140508 |
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 53218-002-02 | 2019-11-27 | C162847 | 48780-1 | 9855d018-d86e-cd31-e053-dbdaa90ab51a | Drug Facts |
| 53218-002-03 | 2019-11-27 | C162847 | 48780-1 | 9855d018-d86e-cd31-e053-dbdaa90ab51a | Drug Facts |
| 53218-002-04 | 2019-11-27 | C162847 | 48780-1 | 9855d018-d86e-cd31-e053-dbdaa90ab51a | Drug Facts |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 53218-002-02 | Total White Brightening | 227 g in 1 JAR | CREAM | 227 | 1 | |
| 53218-002-03 | Total White Brightening | 454 g in 1 JAR | CREAM | 454 | 1 | |
| 53218-002-04 | Total White Brightening | 50 g in 1 TUBE | CREAM | 50 | 1 |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Hydroquinone | ACTIVE INGREDIENT | XV74C1N1AE | 1 | |
| Octinoxate | ACTIVE INGREDIENT | 4Y5P7MUD51 | 1 | |
| Hydroquinone | ACTIVE MOIETY | XV74C1N1AE | 1 | |
| Octinoxate | ACTIVE MOIETY | 4Y5P7MUD51 | 1 | |
| .alpha.-tocopherol Acetate | INACTIVE INGREDIENT | 9E8X80D2L0 | 1 | |
| .beta.-carotene | INACTIVE INGREDIENT | 01YAE03M7J | 1 | |
| Bilberry | INACTIVE INGREDIENT | 9P2U39H18W | 1 | |
| Carrot Seed Oil | INACTIVE INGREDIENT | 595AO13F11 | 1 | |
| Cetyl Alcohol | INACTIVE INGREDIENT | 936JST6JCN | 1 | |
| Coco-caprylate/caprate | INACTIVE INGREDIENT | 8D9H4QU99H | 1 | |
| Corn Oil | INACTIVE INGREDIENT | 8470G57WFM | 1 | |
| Dmdm Hydantoin | INACTIVE INGREDIENT | BYR0546TOW | 1 | |
| Edetate Sodium | INACTIVE INGREDIENT | MP1J8420LU | 1 | |
| Glyceryl Monostearate | INACTIVE INGREDIENT | 230OU9XXE4 | 1 | |
| Kojic Acid | INACTIVE INGREDIENT | 6K23F1TT52 | 1 | |
| Lemon | INACTIVE INGREDIENT | 24RS0A988O | 1 | |
| Methylparaben | INACTIVE INGREDIENT | A2I8C7HI9T | 1 | |
| Orange | INACTIVE INGREDIENT | 5EVU04N5QU | 1 | |
| Pentetic Acid | INACTIVE INGREDIENT | 7A314HQM0I | 1 | |
| Polyethylene Glycol 400 | INACTIVE INGREDIENT | B697894SGQ | 1 | |
| Polyethylene Glycol 4500 | INACTIVE INGREDIENT | TVH7653921 | 1 | |
| Propylene Glycol | INACTIVE INGREDIENT | 6DC9Q167V3 | 1 | |
| Propylparaben | INACTIVE INGREDIENT | Z8IX2SC1OH | 1 | |
| Sodium Metabisulfite | INACTIVE INGREDIENT | 4VON5FNS3C | 1 | |
| Sodium Sulfite | INACTIVE INGREDIENT | VTK01UQK3G | 1 | |
| Stearic Acid | INACTIVE INGREDIENT | 4ELV7Z65AP | 1 | |
| Stearyl Stearate | INACTIVE INGREDIENT | 5WX2EGD0DK | 1 | |
| Sugarcane | INACTIVE INGREDIENT | 81H2R5AOH3 | 1 | |
| Vitamin A Palmitate | INACTIVE INGREDIENT | 1D1K0N0VVC | 1 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | 1 | |
| Xanthan Gum | INACTIVE INGREDIENT | TTV12P4NEE | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 53218-002 | 53218-002-02, 53218-002-03, 53218-002-04 |
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| Propylene Glycol | PROPYLENE GLYCOL | 6DC9Q167V3 | FILM, SOLUBLE / BUCCAL | 5 mg | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | INJECTION / EPIDURAL | 1 mg | ||
| Glyceryl Monostearate | GLYCERYL MONOSTEARATE | 230OU9XXE4 | TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL | 23 mg | ||
| Propylparaben | PROPYLPARABEN | Z8IX2SC1OH | TABLET / ORAL | 0.2 mg | ||
| Corn Oil | CORN OIL | 8470G57WFM | TABLET, DELAYED RELEASE / ORAL | 0.03 mg | ||
| Propylene Glycol | PROPYLENE GLYCOL | 6DC9Q167V3 | SOLUTION/ DROPS / OPHTHALMIC | 0.75 %w/v | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | SOLUTION / IRRIGATION | 2 %w/v | ||
| Glyceryl Monostearate | GLYCERYL MONOSTEARATE | 230OU9XXE4 | TABLET, CHEWABLE / ORAL | 1 mg | ||
| Xanthan Gum | XANTHAN GUM | TTV12P4NEE | SUSPENSION, EXTENDED RELEASE / ORAL | 186.8 mg | ||
| Polyethylene Glycol 400 | POLYETHYLENE GLYCOL 400 | B697894SGQ | TABLET, FILM COATED / ORAL | 20 mg | ||
| Propylparaben | PROPYLPARABEN | Z8IX2SC1OH | INJECTION / SOFT TISSUE | 0.02 %w/v | ||
| Propylparaben | PROPYLPARABEN | Z8IX2SC1OH | EMULSION / TOPICAL | 0.06 %w/w | ||
| Sodium Sulfite | SODIUM SULFITE | VTK01UQK3G | SOLUTION / AURICULAR (OTIC) | 0.02 %w/v | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | OINTMENT / TOPICAL | 29 mg | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | INJECTION / PARENTERAL | 18 mg | ||
| Xanthan Gum | XANTHAN GUM | TTV12P4NEE | TABLET, ORALLY DISINTEGRATING / ORAL | 0.15 mg | ||
| Propylparaben | PROPYLPARABEN | Z8IX2SC1OH | SOLUTION/ DROPS / OPHTHALMIC | 0.01 %w/v | ||
| Xanthan Gum | XANTHAN GUM | TTV12P4NEE | GRANULE, FOR SUSPENSION / ORAL | 450 mg | ||
| Corn Oil | CORN OIL | 8470G57WFM | TABLET / ORAL | 20 mg | ||
| Sodium Metabisulfite | SODIUM METABISULFITE | 4VON5FNS3C | SUSPENSION / TOPICAL | 0.32 %w/v | ||
| Xanthan Gum | XANTHAN GUM | TTV12P4NEE | GEL / TOPICAL | 58 mg | ||
| Xanthan Gum | XANTHAN GUM | TTV12P4NEE | FILM, SOLUBLE / ORAL | 1 mg | ||
| Edetate Sodium | EDETATE SODIUM | MP1J8420LU | INJECTION / INTRAMUSCULAR | 0.01 %w/v | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | SUSPENSION / ORAL | 388 mg | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | PASTE, DENTIFRICE / DENTAL | 0.05 %w/w | ||
| Propylparaben | PROPYLPARABEN | Z8IX2SC1OH | PASTE, DENTIFRICE / DENTAL | NA | ||
| .alpha.-tocopherol Acetate | .ALPHA.-TOCOPHEROL ACETATE | 9E8X80D2L0 | CAPSULE / ORAL | 2 mg | ||
| Stearic Acid | STEARIC ACID | 4ELV7Z65AP | POWDER, FOR SUSPENSION / ORAL | 1203 mg/5ml | ||
| Polyethylene Glycol 400 | POLYETHYLENE GLYCOL 400 | B697894SGQ | EMULSION / TOPICAL | 1.2 %w/w | ||
| Sodium Metabisulfite | SODIUM METABISULFITE | 4VON5FNS3C | INJECTION / INFILTRATION | 0.5 %w/v | ||
| Propylene Glycol | PROPYLENE GLYCOL | 6DC9Q167V3 | INJECTION / INTRAMUSCULAR | 7459 mg | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | INJECTION, SOLUTION / PARENTERAL | 30 mg | ||
| Glyceryl Monostearate | GLYCERYL MONOSTEARATE | 230OU9XXE4 | CAPSULE / ORAL | 13.75 mg | ||
| Propylene Glycol | PROPYLENE GLYCOL | 6DC9Q167V3 | PASTE / DENTAL | 0.5 %w/w | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | GEL / VAGINAL | 8 mg | ||
| Xanthan Gum | XANTHAN GUM | TTV12P4NEE | SUSPENSION / ORAL | 360 mg | ||
| Sodium Metabisulfite | SODIUM METABISULFITE | 4VON5FNS3C | INJECTION / EPIDURAL | 0.05 %w/v | ||
| Propylene Glycol | PROPYLENE GLYCOL | 6DC9Q167V3 | AEROSOL, FOAM / RECTAL | 1214 mg | ||
| Polyethylene Glycol 400 | POLYETHYLENE GLYCOL 400 | B697894SGQ | SUPPOSITORY / RECTAL | 0.25 mg/mg | ||
| Propylene Glycol | PROPYLENE GLYCOL | 6DC9Q167V3 | GEL, METERED / TOPICAL | 1225 mg | ||
| Sodium Sulfite | SODIUM SULFITE | VTK01UQK3G | INJECTION, SOLUTION / INTRAVENOUS | 2 mg | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | INJECTION, SOLUTION / EPIDURAL | 30 mg | ||
| Propylene Glycol | PROPYLENE GLYCOL | 6DC9Q167V3 | EMULSION / OPHTHALMIC | 1.5 %w/v | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | SHAMPOO / TOPICAL | 0.15 %w/w | ||
| Polyethylene Glycol 400 | POLYETHYLENE GLYCOL 400 | B697894SGQ | CAPSULE / ORAL | 13440 mg | ||
| Sodium Sulfite | SODIUM SULFITE | VTK01UQK3G | TABLET / ORAL | 5 mg | ||
| Sodium Sulfite | SODIUM SULFITE | VTK01UQK3G | CREAM / TOPICAL | 8 mg | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | INJECTION / INTRAMUSCULAR | 95 mg | ||
| Polyethylene Glycol 400 | POLYETHYLENE GLYCOL 400 | B697894SGQ | FILM, SOLUBLE / ORAL | 29 mg | ||
| Sodium Metabisulfite | SODIUM METABISULFITE | 4VON5FNS3C | SUSPENSION, EXTENDED RELEASE / ORAL | 100 mg | ||
| Stearic Acid | STEARIC ACID | 4ELV7Z65AP | EMULSION / TOPICAL | NA | ||
| Sodium Sulfite | SODIUM SULFITE | VTK01UQK3G | INJECTION / SOFT TISSUE | 2 mg | ||
| Propylene Glycol | PROPYLENE GLYCOL | 6DC9Q167V3 | SPRAY, METERED / NASAL | 240 mg | ||
| Propylene Glycol | PROPYLENE GLYCOL | 6DC9Q167V3 | SUSPENSION / AURICULAR (OTIC) | 10 %w/v | ||
| Glyceryl Monostearate | GLYCERYL MONOSTEARATE | 230OU9XXE4 | SUPPOSITORY / RECTAL | 35 mg | ||
| Glyceryl Monostearate | GLYCERYL MONOSTEARATE | 230OU9XXE4 | OINTMENT / TOPICAL | 5 %w/w | ||
| Polyethylene Glycol 400 | POLYETHYLENE GLYCOL 400 | B697894SGQ | SPRAY, METERED / NASAL | 320 mg | ||
| Methylparaben | METHYLPARABEN | A2I8C7HI9T | OINTMENT / OPHTHALMIC | 0.05 %w/w | ||
| Xanthan Gum | XANTHAN GUM | TTV12P4NEE | TABLET / ORAL | 56 mg | ||
| Dmdm Hydantoin | DMDM HYDANTOIN | BYR0546TOW | LOTION / TOPICAL | 3 mg |
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 |
|---|---|---|---|---|---|---|
| a1adbdb7-d742-222d-dd33-1d274a198ec1 | 52912284-80b3-c079-d02c-ea62cf164c3e | 2012-06-07 | Warnings | a1adbdb7-d742-222d-dd33-1d274a198ec1 52912284-80b3-c079-d02c-ea62cf164c3e |
Adverse event summaries are temporarily unavailable. Other product information remains available.