COCOOIL SPF 6
- Product NDC
- 72645-004
- 11-digit product format
- 726450004
- Labeler code
- 72645
- Product ID
- 72645-004_ae7f2184-df95-d0ed-e053-2a95a90a0c94
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE, OCTOCRYLENE, OCTOCRYLENE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Cocooil Limited
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-18
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTOCRYLENE; AVOBENZONE
- Active strength
- 40 mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 72645-004-01 | COCOOIL SPF 6 | 100 mL in 1 BOTTLE | LOTION | 100 | | 1 |
| 72645-004-02 | COCOOIL SPF 6 | 200 mL in 1 BOTTLE | LOTION | 200 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72645-004 | COCOOIL SPF 6 (OCTINOXATE, OCTOCRYLENE, OCTOCRYLENE) LOTION [COCOOIL LIMITED] | 1 | Legacy NDC, 2 package rows | 20200905_1199d46b-36a5-4908-9e2c-b85bae27fdca.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72645-004-01 | 72645000401 | 100 mL in 1 BOTTLE (72645-004-01) | 100 ml | 2020-03-18 | 0000-00-00 | No | No | Current |
| 72645-004-02 | 72645000402 | 200 mL in 1 BOTTLE (72645-004-02) | 200 ml | 2020-03-18 | 0000-00-00 | No | No | Current |