SKIN 79 Super Plus Beblesh Balm Triple Functions SPF25 PA (40g)
- Manufacturer
- WIZCOZ CORPORATION LTD
- Effective date
- 2009-11-09
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:23:03
Label at a glance#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
INGREDIENTS:
WATER, PROPYLENE GLYCOL, CYCLOMETHICONE, DIMETHICONE, TITANIUM DIOXIDE, ISOPROPYL PALMITATE, TALC, ETHYLHEXYL METHOXYCINNAMATE, BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE, PRUNUS AMYGDALUS DIACIS (SWEET ALMOND) OIL, ETHYLHEXYL SALICYLATE, DIPENTAERYTHRITYL HEXAHYDROXYSTEARATE/HEXASTEARATE/HEXAROSINATE, CETYL PEG/PPG-10/1 DIMETHICONE, ARBUTIN, ZINC OXIDE, POLYGLYCERYL-4 ISOSTEARATE, MAGNESIUM SULFATE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, IRON OXIDES, SILICA, VINYL DIMETHICONE/METHICONE SISSESQUIOXANE CROSSPOLYER, PORTULACA OLERACEA EXTRACT, PIPER METHYSTICUM LEAF/ROOT/STEM EXTRACT, PHENOSYETHANOL, TRIHYDROXYSTEARIN, DISTEARDIMONIUM HECTORITE, GLYCOSYL TREMALOSE, ALUMINUM HYDROXIDE, ALUMINUM STEARATE, METHYLPARABEN, HYDROGENATED STARCH HYDROLYSATE, METHICONE, TOCOPHEYL ACETATE, HYDROGENATED LECITHIN, NELUMBO NUCIFERA FLOWER WATER, MADECASSOSIDE, CAMELLIA SINENSIS LEAF EXTRACT, ALOE BARBEDENSIS LEAF JUICE, CHOLESTEROL, CERAMIDE 3, LYCIUM CHINENSE FRUTI EXTRACT, HELIANTHUS ANNUUS (SUNFLOWER) EXTRACT, SCHIZANDRA CHINENSIS FRUIT EXTRACT, HEDERA HELIX (IVY) EXTRACT, CORNUS OFFICINALIS FRUIT EXTRACT, FRAGRANCE, PROPYLPARABEN, BUTYLPARABEN, GLYCERIN, ADENOSINE, CAPRYLIC/CAPRIC TRIGLYCERIDE, TRICLOSAN, PHYTIC ACID, UBIQUINONE, BHT
OTC - WHEN USING SECTION
DIRECTIONS:
Use it proper quantity on the area of your face like patting at the last step of skin care.
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 49715-005-01 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-c627-621f-e053-dbdaa90a74ad | 4c4bd37f-a6ff-49e4-b46e-9df4c86d68ab |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49715-005-01 | SKIN 79 Super Plus Beblesh Balm Triple Functions SPF25 PA (40g) | 40 g in 1 BOTTLE, PLASTIC | CREAM | 40 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 49715-005 | SKIN 79 SUPER PLUS BEBLESH BALM TRIPLE FUNCTIONS SPF25 PA (40G) (ZINC OXIDE, OCTISALATE, TITANIUM DIOXIDE) CREAM [WIZCOZ CORPORATION LTD] | 1 | Legacy NDC, 1 package rows | 20091220_4c4bd37f-a6ff-49e4-b46e-9df4c86d68ab.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| OCTINOXATE | ACTIVE INGREDIENT | 4Y5P7MUD51 | 1 | |
| OCTISALATE | ACTIVE INGREDIENT | 4X49Y0596W | 1 | |
| TITANIUM DIOXIDE | ACTIVE INGREDIENT | 15FIX9V2JP | 1 | |
| ZINC OXIDE | ACTIVE INGREDIENT | SOI2LOH54Z | 1 | |
| OCTINOXATE | ACTIVE MOIETY | 4Y5P7MUD51 | 1 | |
| OCTISALATE | ACTIVE MOIETY | 4X49Y0596W | 1 | |
| TITANIUM | ACTIVE MOIETY | D1JT611TNE | 1 | |
| ZINC | ACTIVE MOIETY | J41CSQ7QDS | 1 | |
| ALUMINUM HYDROXIDE | INACTIVE INGREDIENT | 5QB0T2IUN0 | 1 | |
| DIMETHICONE | INACTIVE INGREDIENT | 92RU3N3Y1O | 1 |
Products#
Every source-derived product name is available through these pages.
- SKIN 79 Super Plus Beblesh Balm Triple Functions SPF25 PA (40g)
- ZINC OXIDE, OCTISALATE, TITANIUM DIOXIDE
- DIMETHICONE
- ALUMINUM HYDROXIDE
- ZINC OXIDE
- ZINC
- OCTISALATE
- OCTINOXATE
- TITANIUM DIOXIDE
- TITANIUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 49715-005 | 49715-005-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DIMETHICONE | 92RU3N3Y1O | IACT |
| ALUMINUM HYDROXIDE | 5QB0T2IUN0 | IACT |
| ZINC OXIDE | SOI2LOH54Z | ACTIB |
| OCTISALATE | 4X49Y0596W | ACTIB |
| OCTINOXATE | 4Y5P7MUD51 | ACTIB |
| TITANIUM DIOXIDE | 15FIX9V2JP | ACTIB |
Source Document#
Inactive ingredient matches#
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 |
|---|---|---|---|---|---|---|
| ALUMINUM HYDROXIDE | ALUMINUM HYDROXIDE | 5QB0T2IUN0 | CAPSULE / ORAL | NA | ||
| ALUMINUM HYDROXIDE | ALUMINUM HYDROXIDE | 5QB0T2IUN0 | TABLET / ORAL | 50 mg | ||
| ALUMINUM HYDROXIDE | ALUMINUM HYDROXIDE | 5QB0T2IUN0 | OINTMENT / TOPICAL | NA | ||
| ALUMINUM HYDROXIDE | ALUMINUM HYDROXIDE | 5QB0T2IUN0 | CREAM / TOPICAL | 5 %w/w |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 3ef970da-b81a-4e01-8022-f940d4e08f45 | 4c4bd37f-a6ff-49e4-b46e-9df4c86d68ab | 2009-11-09 | 3ef970da-b81a-4e01-8022-f940d4e08f45 4c4bd37f-a6ff-49e4-b46e-9df4c86d68ab |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
