Vanilla Sunscreen Lip Moisturizer
- Product NDC
- 75866-307
- 11-digit product format
- 758660307
- Labeler code
- 75866
- Product ID
- 75866-307_c2ffc690-8b5b-41d5-8587-47dae254ad9c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE, OXYBENZONE
- Dosage form
- LIPSTICK
- Route
- TOPICAL
- Labeler
- Beacon Promotions, Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-12-29
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OXYBENZONE
- Active strength
- 7 g/100g; g/100g
- 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 |
|---|
| 75866-307-01 | Vanilla Sunscreen Lip Moisturizer | 4.2 g in 1 CONTAINER | LIPSTICK | 4.2 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75866-307 | VANILLA SUNSCREEN LIP MOISTURIZER (OCTINOXATE, OXYBENZONE) LIPSTICK [BEACON PROMOTIONS, INC.] | 1 | Legacy NDC, 1 package rows | 20101230_43dd3933-a254-466f-9414-f63c179921b9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 75866-307-01 | 75866030701 | 4.2 g in 1 CONTAINER | 4.2 g | Historical |