OTC - ACTIVE INGREDIENT SECTION
HOMOSALATE
OCTINOXATE
OCTISALATE
Secret Dig Whitening Sunscreen Spray. SPF50 PA
- Manufacturer
- Yiwu Mijue electronic Commerce Co., LTD
- Effective date
- 2024-07-09
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 00:14:58
Label at a glance#
ProductSecret Dig Whitening Sunscreen Spray. SPF50 PA
Active ingredientHOMOSALATE, OCTISALATE, OCTINOXATE
Label structure9 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
A lightweight sunscreen spray specially designed foroutdoor use can effectively block the exposure of UVA andUVB,evenly cover the skin, with fresh texture, and can breapplied at any time.lt is fresh and not greasy, and can formsunscreen isolation layer on the surface of the skin to providesunscreen care.
INDICATIONS & USAGE SECTION
A lightweight sunscreen spray specially designed for outdoor use can effectively block the exposure of UVA and UVB
Usage:Shake well before use,10-15cm away from the skin and spray evenly on the skin exposed to sunlight(hands,legs,neck,back)
DOSAGE & ADMINISTRATION SECTION
Store in a ventilated and dry environmen below 50 °c, avoid direct sunlight, and keep away from fire and heat sources.
Net:150ml
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Please keep out of reach of infants and young children
RECENT MAJOR CHANGES SECTION
Store in a ventilated and dry environmen below 50 °c, avoid direct sunlight, and keep away from fire and heat sources.
Net:150ml
WARNINGS SECTION
Warning:For external use only,please do not ch e mouh,nose or eyes,do not use in areas with skin damage inflammation or itching
INACTIVE INGREDIENT SECTION
DECYL GLUCOSIDE
BISOCTRIZOLE
WATER
DEHYDROXANTHAN GUM
N-SALICYLOYLGLYCINE
BEMOTRIZINOL
ETHYLHEXYL TRIAZONE
2-PHENYLPROPANAL PROPYLENE GLYCOL ACETAL
OCTOCRYLENE
ZINC OXIDE
STEARIC ACID
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 84462-458-01 | 2025-07-29 | C162847 | 48780-1 | 3b156c62-2fb0-fb37-e063-e6dba90a4e07 | 84462-458 蜜掘电子 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84462-458-01 | Secret Dig Whitening Sunscreen Spray. SPF50 PA | 150 mL in 1 BOTTLE, SPRAY | AEROSOL, SPRAY | 150 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 84462-458 | SECRET DIG WHITENING SUNSCREEN SPRAY. SPF50 PA (SECRET DIG WHITENING SUNSCREEN SPRAY SPF50 PA) AEROSOL, SPRAY [YIWU MIJUE ELECTRONIC COMMERCE CO., LTD] | 1 | 1 package rows | 20240711_1cdbde57-fba6-bfad-e063-6394a90ab4d7.zip |
Products#
Every source-derived product name is available through these pages.
- Secret Dig Whitening Sunscreen Spray. SPF50 PA
- Secret Dig Whitening Sunscreen Spray SPF50 PA
- DECYL GLUCOSIDE
- BISOCTRIZOLE
- WATER
- DEHYDROXANTHAN GUM
- N-SALICYLOYLGLYCINE
- BEMOTRIZINOL
- ETHYLHEXYL TRIAZONE
- 2-PHENYLPROPANAL PROPYLENE GLYCOL ACETAL
- OCTOCRYLENE
- ZINC OXIDE
- STEARIC ACID
- HOMOSALATE
- OCTISALATE
- OCTINOXATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 84462-458 | 84462-458-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DECYL GLUCOSIDE | Z17H97EA6Y | IACT |
| BISOCTRIZOLE | 8NT850T0YS | IACT |
| WATER | 059QF0KO0R | IACT |
| DEHYDROXANTHAN GUM | 63ZP7I1BQO | IACT |
| N-SALICYLOYLGLYCINE | 5BR3P7J05U | IACT |
| BEMOTRIZINOL | PWZ1720CBH | IACT |
| ETHYLHEXYL TRIAZONE | XQN8R9SAK4 | IACT |
| 2-PHENYLPROPANAL PROPYLENE GLYCOL ACETAL | 1ZRR9A405A | IACT |
| OCTOCRYLENE | 5A68WGF6WM | IACT |
| ZINC OXIDE | SOI2LOH54Z | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| HOMOSALATE | V06SV4M95S | ACTIB |
| OCTISALATE | 4X49Y0596W | ACTIB |
| OCTINOXATE | 4Y5P7MUD51 | ACTIB |
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 |
|---|---|---|---|---|---|---|
| 1cdbf10d-34ac-2c89-e063-6394a90ae223 | 1cdbde57-fba6-bfad-e063-6394a90ab4d7 | 2024-07-09 | Warnings | 1cdbf10d-34ac-2c89-e063-6394a90ae223 1cdbde57-fba6-bfad-e063-6394a90ab4d7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.