daily moisturizer
- Product NDC
- 41250-889
- 11-digit product format
- 412500889
- Labeler code
- 41250
- Product ID
- 41250-889_e93e59b7-fe34-4e8e-a64a-bcda930d4394
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Octisalate
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Meijer Distribution, INC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-04-26
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; OCTINOXATE; OCTISALATE
- Active strength
- 30 mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41250-889 | DAILY MOISTURIZER (OCTINOXATE, OCTISALATE) LOTION [MEIJER DISTRIBUTION, INC] | 13 | Legacy NDC | 20240820_6323895d-ca2c-4e4b-9428-a4344b3ec6ab.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41250-889-26 | 41250088926 | 1 BOTTLE, PLASTIC in 1 CARTON (41250-889-26) > 118 mL in 1 BOTTLE, PLASTIC | 2018-04-26 | 0000-00-00 | No | No | Current |