gp sunscreen
- Product NDC
- 71153-2000
- 11-digit product format
- 711532000
- Labeler code
- 71153
- Product ID
- 71153-2000_444a04b9-c143-2c14-e054-00144ff8d46c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone,Homosalate,Octisalate,Octocrylene
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Cross-Brands Manufacturing, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-12-23
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 3 g/mL; g/mL; g/mL; g/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 71153-2000-1 | gp sunscreen | 237 mL in 1 BOTTLE | LOTION | 237 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71153-2000 | GP SUNSCREEN (AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE) LOTION [CROSS-BRANDS MANUFACTURING, LLC] | 1 | Legacy NDC, 1 package rows | 20161223_444a04b9-c142-2c14-e054-00144ff8d46c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 71153-2000-1 | 71153200001 | 237 mL in 1 BOTTLE | 237 ml | Historical |