SPF30 SUNSCREEN
- Product NDC
- 71642-016
- 11-digit product format
- 716420016
- Labeler code
- 71642
- Product ID
- 71642-016_5d55e918-98ba-4989-e053-2a91aa0a9ad7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTISALATE, OCTISALATE, OXYBENZONE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Shanghai Mengna Personal Care Co., Ltd
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-11-06
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE
- Active strength
- 75 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 71642-016-00 | SPF30 SUNSCREEN | 30 mL in 1 BOTTLE | LOTION | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71642-016 | SPF30 SUNSCREEN (OCTISALATE, OCTISALATE, OXYBENZONE) LOTION [SHANGHAI MENGNA PERSONAL CARE CO., LTD] | 2 | Legacy NDC, 1 package rows | 20171106_12aa606e-8e8f-4b21-9dd6-e6d455e21669.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 71642-016-00 | 71642001600 | 30 mL in 1 BOTTLE | 30 ml | Historical |