No Makeup Foundation (Ivory) SPF20
- Manufacturer
- NV Perricone LLC
- Effective date
- 2022-05-19
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 6
- Source
- full-release
- Hydrated at
- 2026-05-31 23:49:39
Label at a glance#
ProductNo Makeup Foundation (Tan) SPF20
Active ingredientZINC OXIDE
Label structure7 sections
Label contents#
Full prescribing information#
INACTIVE INGREDIENT SECTION
INDICATIONS & USAGE SECTION
OTC - ACTIVE INGREDIENT SECTION
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
OTC - PURPOSE SECTION
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0604079161961 | GTIN-13: 0604079161961 EAN-13: 0604079161961 GTIN-12: 604079161961 UPC-A: 604079161961 GTIN storage (14 digits): 00604079161961 | OTC-Purpose.jpg, Package Label Principle Display Panel.jpg, Indications Usage.jpg, OTC-Keep out of reach of Children.jpg, Dosage Administration.jpg, Inactive Ingredients.jpg |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 45634-473-21 | 2024-01-30 | C162847 | 48780-1 | 1030e365-1a58-111a-e063-dadaa90a10e2 | ddc860a7-af8c-faac-e053-2a95a90a555b |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 45634-473-21 | No Makeup Foundation (Tan) SPF20 | 50.8 g in 1 BOTTLE, PUMP | LIQUID | 50.8 | 6 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- No Makeup Foundation (Tan) SPF20
- Zinc Oxide
- OCTYLDODECANOL
- GLYCERIN
- HEPTYL UNDECYLENATE
- POLYSORBATE 60
- HYDRATED SILICA
- EDETATE DISODIUM ANHYDROUS
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
- PHENYLETHYL ALCOHOL
- BELLIS PERENNIS
- WATER
- ISOHEXADECANE
- PHENOXYETHANOL
- CAPRYLYL GLYCOL
- CETYL ALCOHOL
- XANTHAN GUM
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS
- POTASSIUM CHLORIDE
- POTASSIUM PHOSPHATE, UNSPECIFIED FORM
- PALMITOYL TRIPEPTIDE-1
- FERROUS OXIDE
- TRIETHOXYCAPRYLYLSILANE
- POTASSIUM SORBATE
- BUTYLENE GLYCOL
- PALMITOYL TETRAPEPTIDE-7
- SODIUM CHLORIDE
- CITRIC ACID MONOHYDRATE
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE)
- BUTYLOCTYL SALICYLATE
- PEG-10 STEARATE
- POLYSORBATE 20
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%)
- HEXYLENE GLYCOL
- GLYCERYL STEARATE/PEG-100 STEARATE
- SORBITAN ISOSTEARATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 45634-473 | 45634-473-21 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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 |
|---|---|---|---|---|---|---|
| df623d95-e200-38a6-e053-2a95a90a1690 | ddc860a7-af8c-faac-e053-2a95a90a555b | 2022-05-19 | df623d95-e200-38a6-e053-2a95a90a1690 ddc860a7-af8c-faac-e053-2a95a90a555b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.






