SunBurnt Advanced After-Sun
- Product NDC
- 0295-1107
- 11-digit product format
- 002951107
- Labeler code
- 0295
- Product ID
- 0295-1107_d92fb973-8195-44f1-a33a-cddcace9259e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Denison Pharmaceuticals, LLC.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2007-01-01
- Marketing end
- 0000-00-00
- Substance
- CALENDULA OFFICINALIS FLOWER; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA
- Active strength
- 1 [hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0295-1107-24 | 00295110724 | 1 TUBE in 1 CARTON (0295-1107-24) > 170 g in 1 TUBE | 1 tube | 2017-01-01 | 0000-00-00 | No | No | Current |
| 0295-1107-45 | 00295110745 | 1 TUBE in 1 CARTON (0295-1107-45) > 71 g in 1 TUBE | 1 tube | 2017-01-01 | 0000-00-00 | No | No | Current |