I-MAX LIGHTENING 5
- Product NDC
- 42952-201
- 11-digit product format
- 429520201
- Labeler code
- 42952
- Product ID
- 42952-201_8c9b94d9-1ae4-4def-bdb0-78aeba442a31
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- HYDROQUINONE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- MAXLIFE USA, INC.
- Application
- part358A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2012-09-18
- Marketing end
- 0000-00-00
- Substance
- HYDROQUINONE
- Active strength
- 2 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42952-201-12 | I-MAX LIGHTENING 5 | 59 g in 1 TUBE | CREAM | 59 | | 6 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| HYDROQUINONE | ACTIVE INGREDIENT | XV74C1N1AE | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| HYDROQUINONE | ACTIVE MOIETY | XV74C1N1AE | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| C13-14 ISOPARAFFIN | INACTIVE INGREDIENT | E4F12ROE70 | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| CETYL ALCOHOL | INACTIVE INGREDIENT | 936JST6JCN | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| ETHYLHEXYL STEARATE | INACTIVE INGREDIENT | EG3PA2K3K5 | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| ETHYLHEXYLGLYCERIN | INACTIVE INGREDIENT | 147D247K3P | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| GLYCERIN | INACTIVE INGREDIENT | PDC6A3C0OX | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| GLYCERYL MONOSTEARATE | INACTIVE INGREDIENT | 230OU9XXE4 | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| GLYCOLIC ACID | INACTIVE INGREDIENT | 0WT12SX38S | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| ISOPROPYL MYRISTATE | INACTIVE INGREDIENT | 0RE8K4LNJS | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| LAURETH-7 | INACTIVE INGREDIENT | Z95S6G8201 | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| NIACINAMIDE | INACTIVE INGREDIENT | 25X51I8RD4 | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| PANTOTHENIC ACID | INACTIVE INGREDIENT | 19F5HK2737 | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| PEG-100 STEARATE | INACTIVE INGREDIENT | YD01N1999R | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| PHENOXYETHANOL | INACTIVE INGREDIENT | HIE492ZZ3T | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| POLYACRYLAMIDE (10000 MW) | INACTIVE INGREDIENT | E2KR9C9V2I | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| PYRIDOXINE HYDROCHLORIDE | INACTIVE INGREDIENT | 68Y4CF58BV | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| SODIUM METABISULFITE | INACTIVE INGREDIENT | 4VON5FNS3C | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| TETRAHEXYLDECYL ASCORBATE | INACTIVE INGREDIENT | 9LBV3F07AZ | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
| XANTHAN GUM | INACTIVE INGREDIENT | TTV12P4NEE | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 2 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42952-201 | I-MAX LIGHTENING 5 (HYDROQUINONE) CREAM [MAXLIFE USA, INC.] | 6 | Legacy NDC, 1 package rows | 20181107_e874f160-1f05-4f53-8e41-8d41c2b441d8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 42952-201-12 | 42952020112 | 59 g in 1 TUBE | 59 g | Historical |