DR.TEEN Day Time Repair
- Product NDC
- 87964-002
- 11-digit product format
- 879640002
- Labeler code
- 87964
- Product ID
- 87964-002_5bc4bdd4-fe05-6b58-e063-6294a90aabc7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allantoin Dimethicone Glycerin
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Guangzhou Oulan Cosmetics Co., Ltd.
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-18
- Substance
- DIMETHICONE; ALLANTOIN; GLYCERIN
- Active strength
- 2; .3; 5 g/100g; g/100g; g/100g
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC], Skin Barrier Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DR.TEEN Day Time Repair
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| DIMETHICONE | 2 g/100g |
| ALLANTOIN | .3 g/100g |
| GLYCERIN | 5 g/100g |
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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 87964-002-01 | 87964000201 | 20 g in 1 BOTTLE (87964-002-01) | 20 g | 2026-09-18 | No | No | Current |