General Protection
- Product NDC
- 71153-2008
- 11-digit product format
- 711532008
- Labeler code
- 71153
- Product ID
- 71153-2008_7ef772ff-3e5d-5b1c-e053-2a91aa0a35e7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone,Octisalate,Octocrylene,Homosalate
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- Cross-Brands Manufacturing LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-01-04
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; OCTISALATE; OCTINOXATE; OCTOCRYLENE; HOMOSALATE
- Active strength
- 3 g/g; g/g; g/g; g/g; g/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71153-2008-1 | General Protection | 170 g in 1 CAN | AEROSOL, SPRAY | 170 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71153-2008 | GENERAL PROTECTION (AVOBENZONE,OCTISALATE,OCTOCRYLENE,HOMOSALATE) AEROSOL, SPRAY [CROSS-BRANDS MANUFACTURING LLC] | 2 | Legacy NDC, 1 package rows | 20190109_455004c4-9601-584d-e054-00144ff8d46c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 71153-2008-1 | 71153200801 | 170 g in 1 CAN | 170 g | Historical |