Mentholatum Natural Ice - Original, SPF 15
- Product NDC
- 10742-3070
- 11-digit product format
- 107423070
- Labeler code
- 10742
- Product ID
- 10742-3070_4dd2d60a-169b-d3a6-e063-6294a90a6acc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- dimethicone, octinoxate, octisalate
- Dosage form
- STICK
- Route
- TOPICAL
- Labeler
- The Mentholatum Company
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-09-01
- Substance
- DIMETHICONE; OCTINOXATE; OCTISALATE
- Active strength
- 10; 75; 50 mg/g; mg/g; mg/g
- Pharmacologic classes
- Skin Barrier Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mentholatum Natural Ice - Original, SPF 15
- Brand name suffix
- Original
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIMETHICONE | 10 mg/g |
| OCTINOXATE | 75 mg/g |
| OCTISALATE | 50 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 92RU3N3Y1O, 4Y5P7MUD51, 4X49Y0596W |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10742-3070-1 | Mentholatum Natural Ice - Original, SPF 15Original | 1 in 1 BLISTER PACK | STICK | 1 | | 3 |
| 10742-3070-1 | Mentholatum Natural Ice - Original, SPF 15Original | 4.2 g in 1 TUBE | STICK | 4.2 | | 3 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 10742-3070-1 | 10742307001 | 1 TUBE in 1 BLISTER PACK (10742-3070-1) / 4.2 g in 1 TUBE | 1 tube | 2024-09-01 | No | No | Historical |