SUNSCREEN MOISTURIZER
- Product NDC
- 46007-203
- 11-digit product format
- 460070203
- Labeler code
- 46007
- Product ID
- 46007-203_4642868b-77c1-411e-e063-6394a90ac676
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE HOMOSALATE OCTOCRYLENE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Skin Authority LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2012-04-19
- Substance
- AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
- Active strength
- 3; 7; 7.5; 5; 3; 6 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 46007-203-21 | SUNSCREEN MOISTURIZERSPF 30 | 20 mL in 1 TUBE | LOTION | 20 | | 8 |
| 46007-203-24 | SUNSCREEN MOISTURIZERSPF 30 | 118 mL in 1 TUBE | LOTION | 118 | | 8 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 46007-203 | SUNSCREEN MOISTURIZER SPF 30 (AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE HOMOSALATE OCTOCRYLENE) LOTION [SKIN AUTHORITY LLC] | 7 | Current NDC, Legacy NDC, 2 package rows | 20250110_522ed1ed-4935-4b7c-a21a-ebd697a9a749.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 46007-203-21 | 46007020321 | 20 mL in 1 TUBE (46007-203-21) | 20 ml | 2012-04-19 | 0000-00-00 | No | No | Current |
| 46007-203-24 | 46007020324 | 118 mL in 1 TUBE (46007-203-24) | 118 ml | 2012-04-19 | 0000-00-00 | No | No | Current |