NDC 11697-372-01 - Flawless by Sonya Aloe BB Creme Sandy
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 11697-372
- Requested NDC
- 11697-372-01
- Package NDCs from labels
- 11697-372-01, 11697-372-02
- Manufacturer
- Aloe Vera of America, Inc.
- Effective date
- 2015-01-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Flawless by Sonya Aloe BB Creme Sandy - Aloe Vera of America, Inc. | Aloe Vera of America, Inc. | 2015-01-22 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 11697-372-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-857e-f424-e053-dadaa90a57ce | e2bd982e-3e5b-4857-9af0-087abe92de9f |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11697-372-01 | Flawless by Sonya Aloe BB CremeSandy | 45 g in 1 TUBE | CREAM | 45 | 3 | |
| 11697-372-02 | Flawless by Sonya Aloe BB CremeSandy | 1 in 1 CARTON | CREAM | 1 | 3 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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.
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| Plus Rinse Emergency Eyewash | PURIFIED WATER | INNOVATIVE SAFETY SUPPLY INC. | b3f47d26-39e4-4aea-bb92-358def52b652 | 2026-01-08 | Warnings | 059QF0KO0R |
| pH Neutral Emergency Eyewash | WATER | INNOVATIVE SAFETY SUPPLY INC. | 29a1bd1e-d0dd-478f-e063-6394a90ab0aa | 2026-01-08 | Warnings | 059QF0KO0R |
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| Metab 6012 | METAB | Professional Complementary Health Formulas | f3576d6f-c9ab-4370-8a32-b6c4bf6ba4fd | 2026-01-08 | Warnings | 451W47IQ8X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.