GOODAL HEARTLEAF SOOTHING ZINC 100 MINERAL SUNSCREEN
- Product NDC
- 84532-003
- 11-digit product format
- 845320003
- Labeler code
- 84532
- Product ID
- 84532-003_4d560b05-0389-1391-e063-6394a90a3bae
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- CLIO COSMETICS Co., Ltd.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-03-15
- Substance
- ZINC OXIDE
- Active strength
- 219.606 mg/mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- GOODAL HEARTLEAF SOOTHING ZINC 100 MINERAL SUNSCREEN
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 219.606 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SOI2LOH54Z |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84532-003-01 | GOODAL HEARTLEAF SOOTHING ZINC 100 MINERAL SUNSCREEN | 50 mL in 1 TUBE | CREAM | 50 | | 1 |
| 84532-003-02 | GOODAL HEARTLEAF SOOTHING ZINC 100 MINERAL SUNSCREEN | 1 in 1 CARTON | CREAM | 1 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84532-003-01 | 84532000301 | 50 mL in 1 TUBE | 50 ml | | | | Historical |
| 84532-003-02 | 84532000302 | 1 TUBE in 1 CARTON (84532-003-02) / 50 mL in 1 TUBE (84532-003-01) | 1 tube | 2026-03-15 | No | No | Historical |